In the title compound, C11H14O2, the tetrahydropyran ring adopts a 1C4 conformation, with the phenyl and the hydroxy substituents located in equatorial positions. Hydrogen bonding occurs in the solid state between hydroxy groups to link two molecules of (R,R)-trans-4-phenylperhydropyran-3-ol and two molecules of the (S,S)-enantiomer to provide tetramers.
Supporting information
CCDC reference: 282574
Key indicators
- Single-crystal X-ray study
- T = 299 K
- Mean (C-C) = 0.005 Å
- R factor = 0.062
- wR factor = 0.208
- Data-to-parameter ratio = 15.5
checkCIF/PLATON results
No syntax errors found
Alert level B
RINTA01_ALERT_3_B The value of Rint is greater than 0.15
Rint given 0.160
PLAT020_ALERT_3_B The value of Rint is greater than 0.10 ......... 0.16
Alert level C
SHFSU01_ALERT_2_C The absolute value of parameter shift to su ratio > 0.05
Absolute value of the parameter shift to su ratio given 0.068
Additional refinement cycles may be required.
PLAT026_ALERT_3_C Ratio Observed / Unique Reflections too Low .... 48 Perc.
PLAT048_ALERT_1_C MoietyFormula Not Given ........................ ?
PLAT080_ALERT_2_C Maximum Shift/Error ............................ 0.07
PLAT125_ALERT_4_C No _symmetry_space_group_name_Hall Given ....... ?
PLAT340_ALERT_3_C Low Bond Precision on C-C bonds (x 1000) Ang ... 5
PLAT417_ALERT_2_C Short Inter D-H..H-D H2C .. H4A .. 2.10 Ang.
PLAT790_ALERT_4_C Centre of Gravity not Within Unit Cell: Resd. # 2
C11 H14 O2
0 ALERT level A = In general: serious problem
2 ALERT level B = Potentially serious problem
8 ALERT level C = Check and explain
0 ALERT level G = General alerts; check
1 ALERT type 1 CIF construction/syntax error, inconsistent or missing data
3 ALERT type 2 Indicator that the structure model may be wrong or deficient
4 ALERT type 3 Indicator that the structure quality may be low
2 ALERT type 4 Improvement, methodology, query or suggestion
Data collection: CAD-4 Diffractometer Control Software (Nonius, 1993); cell refinement: CAD-4 Diffractometer Control Software; data reduction: CAD-4 Diffractometer Control Software; program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: PLATON (Spek, 1990; Spek 2003) and ORTEP-3 for Windows (Farrugia,
1997, 2005); software used to prepare material for publication: SHELXL97.
trans-4-Phenyl-3-tetrahydropyranol
top
Crystal data top
C11H14O2 | F(000) = 384 |
Mr = 178.22 | Dx = 1.236 Mg m−3 |
Triclinic, P1 | Melting point: 346 K |
a = 9.580 (3) Å | Mo Kα radiation, λ = 0.71073 Å |
b = 10.015 (1) Å | Cell parameters from 25 reflections |
c = 10.670 (2) Å | θ = 2.6–12.4° |
α = 77.38 (1)° | µ = 0.08 mm−1 |
β = 85.68 (2)° | T = 299 K |
γ = 73.55 (1)° | Prism, colourless |
V = 958.0 (4) Å3 | 0.50 × 0.22 × 0.10 mm |
Z = 4 | |
Data collection top
Nonius CAD-4 diffractometer | Rint = 0.160 |
Radiation source: fine-focus sealed tube | θmax = 26.0°, θmin = 4.2° |
Graphite monochromator | h = −11→1 |
ω/2θ scans | k = −12→11 |
4247 measured reflections | l = −13→13 |
3738 independent reflections | 3 standard reflections every 120 min |
1776 reflections with I > 2σ(I) | intensity decay: 13.9% |
Refinement top
Refinement on F2 | Primary atom site location: structure-invariant direct methods |
Least-squares matrix: full | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.062 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.208 | H atoms treated by a mixture of independent and constrained refinement |
S = 0.90 | w = 1/[σ2(Fo2) + (0.113P)2 + 0.3203P] where P = (Fo2 + 2Fc2)/3 |
3738 reflections | (Δ/σ)max = 0.068 |
241 parameters | Δρmax = 0.27 e Å−3 |
0 restraints | Δρmin = −0.32 e Å−3 |
Special details top
Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes)
are estimated using the full covariance matrix. The cell e.s.d.'s are taken
into account individually in the estimation of e.s.d.'s in distances, angles
and torsion angles; correlations between e.s.d.'s in cell parameters are only
used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s.
planes. |
Refinement. Refinement of F2 against ALL reflections. The weighted R-factor
wR and goodness of fit S are based on F2, conventional
R-factors R are based on F, with F set to zero for
negative F2. The threshold expression of F2 >
σ(F2) is used only for calculating R-factors(gt) etc.
and is not relevant to the choice of reflections for refinement.
R-factors based on F2 are statistically about twice as large
as those based on F, and R- factors based on ALL data will be
even larger. |
Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top | x | y | z | Uiso*/Ueq | |
C2 | 0.3676 (4) | 0.3320 (3) | 0.1975 (4) | 0.0485 (8) | |
H2A | 0.3009 | 0.3645 | 0.2645 | 0.058* | |
H2B | 0.4491 | 0.3721 | 0.1944 | 0.058* | |
C3 | 0.4225 (3) | 0.1719 (3) | 0.2311 (3) | 0.0375 (7) | |
H3 | 0.4954 | 0.1412 | 0.1662 | 0.045* | |
C4 | 0.2994 (3) | 0.1027 (3) | 0.2294 (3) | 0.0381 (7) | |
H4 | 0.2307 | 0.1286 | 0.2986 | 0.046* | |
C5 | 0.2184 (4) | 0.1668 (4) | 0.1030 (3) | 0.0477 (8) | |
H5A | 0.2810 | 0.1365 | 0.0328 | 0.057* | |
H5B | 0.1330 | 0.1325 | 0.1054 | 0.057* | |
C6 | 0.1726 (4) | 0.3277 (4) | 0.0797 (4) | 0.0578 (10) | |
H6A | 0.1230 | 0.3658 | −0.0017 | 0.069* | |
H6B | 0.1048 | 0.3580 | 0.1469 | 0.069* | |
C7 | 0.3541 (3) | −0.0594 (3) | 0.2562 (3) | 0.0386 (7) | |
C8 | 0.3338 (4) | −0.1367 (4) | 0.3755 (3) | 0.0500 (9) | |
H8 | 0.2845 | −0.0903 | 0.4391 | 0.060* | |
C9 | 0.3864 (5) | −0.2841 (4) | 0.4021 (4) | 0.0659 (11) | |
H9 | 0.3724 | −0.3356 | 0.4835 | 0.079* | |
C10 | 0.4590 (4) | −0.3542 (4) | 0.3093 (4) | 0.0645 (11) | |
H10 | 0.4934 | −0.4529 | 0.3274 | 0.077* | |
C11 | 0.4802 (4) | −0.2783 (4) | 0.1905 (4) | 0.0601 (10) | |
H11 | 0.5297 | −0.3252 | 0.1273 | 0.072* | |
C12 | 0.4281 (4) | −0.1316 (4) | 0.1635 (3) | 0.0495 (9) | |
H12 | 0.4430 | −0.0807 | 0.0821 | 0.059* | |
C13 | −0.1576 (4) | 0.6642 (4) | 0.3878 (4) | 0.0633 (11) | |
H13A | −0.1032 | 0.6436 | 0.4661 | 0.076* | |
H13B | −0.2415 | 0.6269 | 0.4081 | 0.076* | |
C14 | −0.2087 (3) | 0.8237 (3) | 0.3395 (3) | 0.0442 (8) | |
H14 | −0.2682 | 0.8440 | 0.2633 | 0.053* | |
C15 | −0.0792 (3) | 0.8846 (3) | 0.3036 (3) | 0.0400 (7) | |
H15 | −0.0243 | 0.8658 | 0.3825 | 0.048* | |
C16 | 0.0210 (4) | 0.8020 (4) | 0.2112 (4) | 0.0544 (9) | |
H16A | −0.0267 | 0.8233 | 0.1293 | 0.065* | |
H16B | 0.1098 | 0.8317 | 0.1967 | 0.065* | |
C17 | 0.0577 (4) | 0.6442 (4) | 0.2649 (5) | 0.0733 (13) | |
H17A | 0.1167 | 0.5942 | 0.2026 | 0.088* | |
H17B | 0.1146 | 0.6221 | 0.3419 | 0.088* | |
C18 | −0.1230 (3) | 1.0438 (3) | 0.2552 (3) | 0.0367 (7) | |
C19 | −0.1881 (4) | 1.1069 (4) | 0.1370 (3) | 0.0493 (8) | |
H19 | −0.2044 | 1.0503 | 0.0843 | 0.059* | |
C20 | −0.2289 (4) | 1.2536 (4) | 0.0968 (4) | 0.0601 (10) | |
H20 | −0.2721 | 1.2944 | 0.0172 | 0.072* | |
C21 | −0.2066 (4) | 1.3386 (4) | 0.1725 (4) | 0.0595 (10) | |
H21 | −0.2350 | 1.4370 | 0.1450 | 0.071* | |
C22 | −0.1426 (4) | 1.2789 (4) | 0.2886 (4) | 0.0587 (10) | |
H22 | −0.1273 | 1.3365 | 0.3407 | 0.070* | |
C23 | −0.1001 (4) | 1.1319 (3) | 0.3292 (3) | 0.0463 (8) | |
H23 | −0.0551 | 1.0922 | 0.4082 | 0.056* | |
O1 | 0.2955 (3) | 0.3828 (2) | 0.0779 (2) | 0.0566 (7) | |
O2 | 0.4926 (2) | 0.1316 (2) | 0.3521 (2) | 0.0438 (6) | |
H2C | 0.425 (4) | 0.140 (4) | 0.417 (3) | 0.053* | |
O3 | −0.0685 (3) | 0.5958 (3) | 0.2950 (3) | 0.0810 (10) | |
O4 | −0.2960 (3) | 0.8831 (3) | 0.4378 (2) | 0.0559 (7) | |
H4A | −0.353 (4) | 0.953 (5) | 0.403 (4) | 0.067* | |
Atomic displacement parameters (Å2) top | U11 | U22 | U33 | U12 | U13 | U23 |
C2 | 0.0464 (18) | 0.0401 (19) | 0.059 (2) | −0.0115 (15) | −0.0050 (16) | −0.0090 (16) |
C3 | 0.0375 (16) | 0.0341 (17) | 0.0389 (18) | −0.0084 (12) | 0.0007 (13) | −0.0053 (13) |
C4 | 0.0342 (15) | 0.0366 (17) | 0.0413 (18) | −0.0088 (13) | 0.0014 (13) | −0.0057 (13) |
C5 | 0.0436 (18) | 0.049 (2) | 0.049 (2) | −0.0146 (14) | −0.0096 (15) | −0.0024 (15) |
C6 | 0.050 (2) | 0.051 (2) | 0.064 (2) | −0.0090 (16) | −0.0141 (17) | 0.0053 (18) |
C7 | 0.0366 (16) | 0.0388 (18) | 0.0426 (19) | −0.0143 (13) | −0.0018 (13) | −0.0076 (14) |
C8 | 0.064 (2) | 0.045 (2) | 0.042 (2) | −0.0187 (16) | 0.0001 (16) | −0.0069 (15) |
C9 | 0.095 (3) | 0.048 (2) | 0.055 (2) | −0.029 (2) | −0.010 (2) | 0.0034 (18) |
C10 | 0.076 (3) | 0.035 (2) | 0.083 (3) | −0.0130 (18) | −0.022 (2) | −0.009 (2) |
C11 | 0.065 (2) | 0.050 (2) | 0.066 (3) | −0.0073 (18) | −0.0044 (19) | −0.026 (2) |
C12 | 0.056 (2) | 0.046 (2) | 0.047 (2) | −0.0150 (15) | 0.0040 (16) | −0.0100 (16) |
C13 | 0.056 (2) | 0.037 (2) | 0.095 (3) | −0.0165 (16) | −0.002 (2) | −0.0055 (19) |
C14 | 0.0413 (17) | 0.0396 (18) | 0.052 (2) | −0.0101 (13) | 0.0004 (15) | −0.0119 (15) |
C15 | 0.0418 (17) | 0.0336 (17) | 0.0438 (18) | −0.0072 (13) | −0.0064 (14) | −0.0088 (13) |
C16 | 0.0447 (19) | 0.050 (2) | 0.067 (3) | −0.0060 (15) | 0.0054 (17) | −0.0224 (18) |
C17 | 0.055 (2) | 0.052 (2) | 0.113 (4) | −0.0001 (18) | 0.001 (2) | −0.035 (2) |
C18 | 0.0340 (15) | 0.0357 (17) | 0.0380 (18) | −0.0086 (12) | 0.0035 (13) | −0.0055 (13) |
C19 | 0.0486 (19) | 0.052 (2) | 0.047 (2) | −0.0144 (16) | −0.0041 (15) | −0.0092 (16) |
C20 | 0.048 (2) | 0.062 (3) | 0.054 (2) | −0.0064 (17) | −0.0054 (17) | 0.0122 (19) |
C21 | 0.058 (2) | 0.035 (2) | 0.075 (3) | −0.0101 (16) | 0.011 (2) | 0.0032 (19) |
C22 | 0.074 (2) | 0.041 (2) | 0.067 (3) | −0.0227 (17) | 0.009 (2) | −0.0174 (18) |
C23 | 0.058 (2) | 0.044 (2) | 0.0385 (19) | −0.0157 (15) | −0.0005 (15) | −0.0083 (15) |
O1 | 0.0590 (15) | 0.0442 (14) | 0.0606 (16) | −0.0161 (11) | −0.0118 (12) | 0.0083 (11) |
O2 | 0.0391 (12) | 0.0488 (14) | 0.0418 (14) | −0.0078 (10) | −0.0013 (10) | −0.0114 (10) |
O3 | 0.0712 (19) | 0.0453 (16) | 0.136 (3) | −0.0162 (13) | 0.0084 (18) | −0.0420 (17) |
O4 | 0.0523 (14) | 0.0467 (15) | 0.0536 (16) | −0.0007 (11) | 0.0081 (12) | 0.0013 (12) |
Geometric parameters (Å, º) top
C2—O1 | 1.419 (4) | C13—C14 | 1.514 (5) |
C2—C3 | 1.508 (4) | C13—H13A | 0.9700 |
C2—H2A | 0.9700 | C13—H13B | 0.9700 |
C2—H2B | 0.9700 | C14—O4 | 1.418 (4) |
C3—O2 | 1.424 (4) | C14—C15 | 1.521 (4) |
C3—C4 | 1.531 (4) | C14—H14 | 0.9800 |
C3—H3 | 0.9800 | C15—C18 | 1.510 (4) |
C4—C7 | 1.526 (4) | C15—C16 | 1.530 (4) |
C4—C5 | 1.526 (4) | C15—H15 | 0.9800 |
C4—H4 | 0.9800 | C16—C17 | 1.506 (5) |
C5—C6 | 1.514 (5) | C16—H16A | 0.9700 |
C5—H5A | 0.9700 | C16—H16B | 0.9700 |
C5—H5B | 0.9700 | C17—O3 | 1.416 (5) |
C6—O1 | 1.433 (4) | C17—H17A | 0.9700 |
C6—H6A | 0.9700 | C17—H17B | 0.9700 |
C6—H6B | 0.9700 | C18—C19 | 1.388 (4) |
C7—C8 | 1.370 (4) | C18—C23 | 1.376 (5) |
C7—C12 | 1.386 (4) | C19—C20 | 1.385 (5) |
C8—C9 | 1.389 (5) | C19—H19 | 0.9300 |
C8—H8 | 0.9300 | C20—C21 | 1.361 (6) |
C9—C10 | 1.371 (6) | C20—H20 | 0.9300 |
C9—H9 | 0.9300 | C21—C22 | 1.361 (6) |
C10—C11 | 1.362 (6) | C21—H21 | 0.9300 |
C10—H10 | 0.9300 | C22—C23 | 1.389 (5) |
C11—C12 | 1.383 (5) | C22—H22 | 0.9300 |
C11—H11 | 0.9300 | C23—H23 | 0.9300 |
C12—H12 | 0.9300 | O2—H2C | 0.91 (4) |
C13—O3 | 1.420 (5) | O4—H4A | 0.79 (4) |
| | | |
O1—C2—C3 | 112.9 (3) | C14—C13—H13A | 109.3 |
O1—C2—H2A | 109.0 | O3—C13—H13B | 109.3 |
C3—C2—H2A | 109.0 | C14—C13—H13B | 109.3 |
O1—C2—H2B | 109.0 | H13A—C13—H13B | 108.0 |
C3—C2—H2B | 109.0 | O4—C14—C15 | 111.8 (3) |
H2A—C2—H2B | 107.8 | O4—C14—C13 | 107.7 (3) |
O2—C3—C2 | 108.6 (3) | C15—C14—C13 | 110.5 (3) |
O2—C3—C4 | 112.7 (2) | O4—C14—H14 | 109.0 |
C2—C3—C4 | 111.2 (2) | C15—C14—H14 | 109.0 |
O2—C3—H3 | 108.1 | C13—C14—H14 | 109.0 |
C2—C3—H3 | 108.0 | C18—C15—C16 | 113.9 (3) |
C4—C3—H3 | 108.0 | C18—C15—C14 | 113.0 (2) |
C7—C4—C5 | 113.7 (3) | C16—C15—C14 | 109.0 (3) |
C7—C4—C3 | 112.0 (2) | C18—C15—H15 | 106.8 |
C5—C4—C3 | 108.9 (2) | C16—C15—H15 | 106.8 |
C7—C4—H4 | 107.3 | C14—C15—H15 | 106.8 |
C5—C4—H4 | 107.3 | C17—C16—C15 | 110.8 (3) |
C3—C4—H4 | 107.3 | C17—C16—H16A | 109.5 |
C6—C5—C4 | 111.0 (3) | C15—C16—H16A | 109.5 |
C6—C5—H5A | 109.5 | C17—C16—H16B | 109.5 |
C4—C5—H5A | 109.4 | C15—C16—H16B | 109.5 |
C6—C5—H5B | 109.4 | H16A—C16—H16B | 108.1 |
C4—C5—H5B | 109.4 | O3—C17—C16 | 112.1 (3) |
H5A—C5—H5B | 108.0 | O3—C17—H17A | 109.2 |
O1—C6—C5 | 111.3 (3) | C16—C17—H17A | 109.2 |
O1—C6—H6A | 109.4 | O3—C17—H17B | 109.2 |
C5—C6—H6A | 109.4 | C16—C17—H17B | 109.2 |
O1—C6—H6B | 109.4 | H17A—C17—H17B | 107.9 |
C5—C6—H6B | 109.4 | C19—C18—C23 | 117.6 (3) |
H6A—C6—H6B | 108.0 | C19—C18—C15 | 122.3 (3) |
C8—C7—C12 | 118.4 (3) | C23—C18—C15 | 120.1 (3) |
C8—C7—C4 | 119.9 (3) | C18—C19—C20 | 120.6 (3) |
C12—C7—C4 | 121.7 (3) | C18—C19—H19 | 119.7 |
C7—C8—C9 | 120.4 (3) | C20—C19—H19 | 119.7 |
C7—C8—H8 | 119.8 | C21—C20—C19 | 120.7 (4) |
C9—C8—H8 | 119.8 | C21—C20—H20 | 119.6 |
C8—C9—C10 | 120.5 (4) | C19—C20—H20 | 119.6 |
C8—C9—H9 | 119.7 | C22—C21—C20 | 119.7 (3) |
C10—C9—H9 | 119.7 | C22—C21—H21 | 120.2 |
C11—C10—C9 | 119.5 (4) | C20—C21—H21 | 120.2 |
C11—C10—H10 | 120.2 | C21—C22—C23 | 120.0 (4) |
C9—C10—H10 | 120.2 | C21—C22—H22 | 120.0 |
C10—C11—C12 | 120.2 (4) | C23—C22—H22 | 120.0 |
C10—C11—H11 | 119.9 | C22—C23—C18 | 121.4 (3) |
C12—C11—H11 | 119.9 | C22—C23—H23 | 119.3 |
C7—C12—C11 | 120.9 (3) | C18—C23—H23 | 119.3 |
C7—C12—H12 | 119.5 | C2—O1—C6 | 110.5 (3) |
C11—C12—H12 | 119.5 | C3—O2—H2C | 110 (2) |
O3—C13—C14 | 111.4 (3) | C13—O3—C17 | 111.4 (3) |
O3—C13—H13A | 109.3 | C14—O4—H4A | 107 (3) |
| | | |
O1—C2—C3—O2 | −179.9 (3) | O4—C14—C15—C18 | −59.9 (4) |
O1—C2—C3—C4 | −55.3 (4) | C13—C14—C15—C18 | −179.8 (3) |
O2—C3—C4—C7 | −60.8 (3) | O4—C14—C15—C16 | 172.4 (3) |
C2—C3—C4—C7 | 176.9 (3) | C13—C14—C15—C16 | 52.5 (4) |
O2—C3—C4—C5 | 172.6 (2) | C18—C15—C16—C17 | −179.0 (3) |
C2—C3—C4—C5 | 50.4 (3) | C14—C15—C16—C17 | −51.7 (4) |
C7—C4—C5—C6 | −177.7 (3) | C15—C16—C17—O3 | 55.8 (5) |
C3—C4—C5—C6 | −52.0 (3) | C16—C15—C18—C19 | 54.8 (4) |
C4—C5—C6—O1 | 58.0 (4) | C14—C15—C18—C19 | −70.3 (4) |
C5—C4—C7—C8 | −134.2 (3) | C16—C15—C18—C23 | −125.8 (3) |
C3—C4—C7—C8 | 101.8 (3) | C14—C15—C18—C23 | 109.1 (3) |
C5—C4—C7—C12 | 47.5 (4) | C23—C18—C19—C20 | −0.5 (5) |
C3—C4—C7—C12 | −76.4 (4) | C15—C18—C19—C20 | 178.9 (3) |
C12—C7—C8—C9 | 0.0 (5) | C18—C19—C20—C21 | −0.3 (5) |
C4—C7—C8—C9 | −178.4 (3) | C19—C20—C21—C22 | 0.5 (6) |
C7—C8—C9—C10 | −0.2 (6) | C20—C21—C22—C23 | 0.1 (6) |
C8—C9—C10—C11 | 0.4 (6) | C21—C22—C23—C18 | −0.9 (5) |
C9—C10—C11—C12 | −0.4 (6) | C19—C18—C23—C22 | 1.1 (5) |
C8—C7—C12—C11 | 0.1 (5) | C15—C18—C23—C22 | −178.3 (3) |
C4—C7—C12—C11 | 178.4 (3) | C3—C2—O1—C6 | 59.8 (4) |
C10—C11—C12—C7 | 0.1 (6) | C5—C6—O1—C2 | −60.8 (4) |
O3—C13—C14—O4 | −179.8 (3) | C14—C13—O3—C17 | 60.6 (4) |
O3—C13—C14—C15 | −57.5 (4) | C16—C17—O3—C13 | −59.9 (5) |
Hydrogen-bond geometry (Å, º) top
D—H···A | D—H | H···A | D···A | D—H···A |
O2—H2C···O4i | 0.91 (4) | 1.92 (4) | 2.823 (3) | 168 (3) |
O4—H4A···O2ii | 0.79 (4) | 1.97 (4) | 2.750 (3) | 169 (4) |
Symmetry codes: (i) −x, −y+1, −z+1; (ii) x−1, y+1, z. |