Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536802006384/na6146sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536802006384/na6146Isup2.hkl |
CCDC reference: 185790
Key indicators
- Single-crystal X-ray study
- T = 150 K
- Mean (C-C) = 0.006 Å
- R factor = 0.039
- wR factor = 0.085
- Data-to-parameter ratio = 13.1
checkCIF results
No syntax errors found ADDSYM reports no extra symmetry General Notes
REFLT_03 From the CIF: _diffrn_reflns_theta_max 25.00 From the CIF: _reflns_number_total 2317 Count of symmetry unique reflns 1396 Completeness (_total/calc) 165.97% TEST3: Check Friedels for noncentro structure Estimate of Friedel pairs measured 921 Fraction of Friedel pairs measured 0.660 Are heavy atom types Z>Si present yes Please check that the estimate of the number of Friedel pairs is correct. If it is not, please give the correct count in the _publ_section_exptl_refinement section of the submitted CIF.
The title compound was obtained as a white crystalline solid in 90% yield and 97% enantiomeric excess by treatment of 1,4-dihydro-1,4-epoxynaphthalene in refluxing tetrahydrofuran with 4-bromophenol and a catalyst prepared from [Rh(cyclooctadiene)Cl]2, (R)-(S)-PPF-PtBu2, silver trifluoromethanesulfonate and tetrabutylammonium iodide (Lautens & Fagnou, 2001). Suitable enantiomerically pure crystals were grown from pentane.
With the exception of the hydroxyl H atom, all H atoms were included in calculated positions, with C—H distances of 0.95 and 1.00 Å, and then included in the refinement in riding-motion approximation, with Uiso = 1.2Ueq of the carrier atom. The hydroxyl H atom was refined independently with an isotropic displacement parameter. 921 Friedel pairs were used to determine the absolute stereochemistry.
Data collection: COLLECT (Nonius, 1997-2001); cell refinement: DENZO-SMN (Otwinowski & Minor, 1997); data reduction: DENZO-SMN; program(s) used to solve structure: SHELXTL/PC (Sheldrick, 2001); program(s) used to refine structure: SHELXTL/PC; molecular graphics: SHELXTL/PC; software used to prepare material for publication: SHELXTL/PC.
Fig. 1. View of (I), showing the crystallographic labelling scheme. Ellipsoids are at the 50% probability level. | |
Fig. 2. View of the hydrogen-bonding mode along the a axis in (I). |
C16H13BrO2 | F(000) = 640 |
Mr = 317.17 | Dx = 1.622 Mg m−3 |
Orthorhombic, P212121 | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: P 2ac 2ab | Cell parameters from 1370 reflections |
a = 4.6070 (2) Å | θ = 2.5–25.0° |
b = 11.2898 (4) Å | µ = 3.16 mm−1 |
c = 24.9751 (12) Å | T = 150 K |
V = 1299.01 (10) Å3 | Needle, colourless |
Z = 4 | 0.35 × 0.08 × 0.08 mm |
Nonius KappaCCD diffractometer | 2317 independent reflections |
Radiation source: fine-focus sealed tube | 1897 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.085 |
Detector resolution: 9 pixels mm-1 | θmax = 25.0°, θmin = 3.0° |
ϕ scans, and ω scans with κ offsets | h = −5→5 |
Absorption correction: multi-scan (DENZO-SMN; Otwinowski & Minor, 1997) | k = −13→13 |
Tmin = 0.404, Tmax = 0.786 | l = −29→29 |
6770 measured reflections |
Refinement on F2 | Hydrogen site location: inferred from neighbouring sites |
Least-squares matrix: full | H atoms treated by a mixture of independent and constrained refinement |
R[F2 > 2σ(F2)] = 0.039 | w = 1/[σ2(Fo2) + (0.0189P)2] where P = (Fo2 + 2Fc2)/3 |
wR(F2) = 0.085 | (Δ/σ)max = 0.001 |
S = 1.02 | Δρmax = 0.38 e Å−3 |
2317 reflections | Δρmin = −0.40 e Å−3 |
177 parameters | Extinction correction: SHELXL97, Fc*=kFc[1+0.001xFc2λ3/sin(2θ)]-1/4 |
0 restraints | Extinction coefficient: 0.0039 (10) |
Primary atom site location: structure-invariant direct methods | Absolute structure: (Flack, 1983) |
Secondary atom site location: difference Fourier map | Absolute structure parameter: 0.015 (16) |
C16H13BrO2 | V = 1299.01 (10) Å3 |
Mr = 317.17 | Z = 4 |
Orthorhombic, P212121 | Mo Kα radiation |
a = 4.6070 (2) Å | µ = 3.16 mm−1 |
b = 11.2898 (4) Å | T = 150 K |
c = 24.9751 (12) Å | 0.35 × 0.08 × 0.08 mm |
Nonius KappaCCD diffractometer | 2317 independent reflections |
Absorption correction: multi-scan (DENZO-SMN; Otwinowski & Minor, 1997) | 1897 reflections with I > 2σ(I) |
Tmin = 0.404, Tmax = 0.786 | Rint = 0.085 |
6770 measured reflections |
R[F2 > 2σ(F2)] = 0.039 | H atoms treated by a mixture of independent and constrained refinement |
wR(F2) = 0.085 | Δρmax = 0.38 e Å−3 |
S = 1.02 | Δρmin = −0.40 e Å−3 |
2317 reflections | Absolute structure: (Flack, 1983) |
177 parameters | Absolute structure parameter: 0.015 (16) |
0 restraints |
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. |
x | y | z | Uiso*/Ueq | ||
Br1 | 1.10408 (12) | 0.14084 (4) | 0.275845 (19) | 0.03464 (18) | |
O1 | 0.8052 (7) | 0.2060 (2) | 0.38147 (11) | 0.0269 (8) | |
O2 | 0.6098 (9) | 0.3053 (3) | 0.48223 (12) | 0.0270 (7) | |
H1O | 0.746 (14) | 0.267 (6) | 0.489 (2) | 0.06 (2)* | |
C1 | 0.5733 (11) | 0.2928 (3) | 0.38473 (16) | 0.0224 (10) | |
H1A | 0.3836 | 0.2510 | 0.3895 | 0.027* | |
C2 | 0.6308 (10) | 0.3715 (3) | 0.43340 (14) | 0.0205 (9) | |
H2A | 0.8319 | 0.4042 | 0.4305 | 0.025* | |
C3 | 0.4200 (11) | 0.4731 (3) | 0.43445 (16) | 0.0204 (9) | |
C4 | 0.3122 (10) | 0.5197 (4) | 0.48182 (17) | 0.0244 (11) | |
H4A | 0.3720 | 0.4872 | 0.5151 | 0.029* | |
C5 | 0.1160 (12) | 0.6143 (3) | 0.48096 (18) | 0.0307 (11) | |
H5A | 0.0410 | 0.6447 | 0.5136 | 0.037* | |
C6 | 0.0313 (11) | 0.6634 (4) | 0.43303 (19) | 0.0312 (12) | |
H6A | −0.1006 | 0.7281 | 0.4325 | 0.037* | |
C7 | 0.1398 (11) | 0.6180 (3) | 0.38528 (17) | 0.0288 (11) | |
H7A | 0.0809 | 0.6521 | 0.3523 | 0.035* | |
C8 | 0.3337 (10) | 0.5231 (3) | 0.38509 (16) | 0.0221 (11) | |
C9 | 0.4462 (11) | 0.4736 (4) | 0.33534 (17) | 0.0295 (12) | |
H9A | 0.4360 | 0.5186 | 0.3033 | 0.035* | |
C10 | 0.5626 (11) | 0.3664 (4) | 0.33454 (16) | 0.0274 (11) | |
H10A | 0.6399 | 0.3357 | 0.3021 | 0.033* | |
C12 | 0.7255 (11) | 0.0944 (4) | 0.36361 (18) | 0.0269 (11) | |
C13 | 0.5233 (11) | 0.0274 (4) | 0.39235 (18) | 0.0314 (13) | |
H13A | 0.4347 | 0.0589 | 0.4236 | 0.038* | |
C14 | 0.4533 (13) | −0.0857 (4) | 0.37470 (19) | 0.0360 (14) | |
H14A | 0.3111 | −0.1304 | 0.3934 | 0.043* | |
C15 | 0.5885 (13) | −0.1341 (4) | 0.33018 (19) | 0.0373 (12) | |
H15A | 0.5455 | −0.2129 | 0.3194 | 0.045* | |
C16 | 0.7862 (11) | −0.0671 (4) | 0.30154 (19) | 0.0333 (13) | |
H16A | 0.8773 | −0.0994 | 0.2707 | 0.040* | |
C17 | 0.8513 (12) | 0.0475 (3) | 0.31804 (16) | 0.0275 (11) |
U11 | U22 | U33 | U12 | U13 | U23 | |
Br1 | 0.0337 (3) | 0.0385 (3) | 0.0318 (3) | 0.0004 (3) | 0.0032 (3) | −0.0005 (2) |
O1 | 0.024 (2) | 0.0253 (16) | 0.0318 (17) | 0.0014 (14) | −0.0010 (16) | −0.0055 (13) |
O2 | 0.0236 (19) | 0.0350 (17) | 0.0223 (16) | 0.0048 (18) | 0.0030 (18) | 0.0076 (13) |
C1 | 0.018 (3) | 0.023 (2) | 0.026 (2) | 0.001 (2) | 0.001 (2) | −0.0014 (18) |
C2 | 0.021 (2) | 0.021 (2) | 0.019 (2) | 0.000 (2) | 0.000 (2) | 0.0031 (17) |
C3 | 0.020 (3) | 0.018 (2) | 0.024 (2) | −0.002 (2) | 0.005 (2) | 0.0019 (17) |
C4 | 0.025 (3) | 0.025 (2) | 0.022 (2) | −0.005 (2) | −0.002 (2) | −0.0006 (18) |
C5 | 0.034 (3) | 0.026 (2) | 0.032 (3) | 0.000 (2) | 0.002 (3) | −0.0064 (18) |
C6 | 0.033 (3) | 0.024 (2) | 0.037 (3) | 0.003 (2) | 0.002 (2) | 0.001 (2) |
C7 | 0.030 (3) | 0.023 (2) | 0.033 (3) | −0.009 (2) | −0.002 (3) | 0.0049 (18) |
C8 | 0.026 (3) | 0.018 (2) | 0.023 (2) | −0.007 (2) | −0.002 (2) | 0.0030 (17) |
C9 | 0.031 (3) | 0.034 (3) | 0.023 (2) | −0.004 (2) | −0.002 (2) | 0.0029 (19) |
C10 | 0.036 (3) | 0.027 (2) | 0.020 (2) | 0.001 (3) | −0.001 (2) | −0.0017 (19) |
C12 | 0.030 (3) | 0.025 (2) | 0.026 (3) | −0.002 (2) | −0.007 (2) | −0.0019 (19) |
C13 | 0.041 (4) | 0.028 (3) | 0.025 (3) | −0.003 (2) | −0.005 (2) | 0.001 (2) |
C14 | 0.039 (4) | 0.028 (3) | 0.041 (3) | −0.005 (3) | −0.012 (3) | 0.011 (2) |
C15 | 0.046 (3) | 0.023 (2) | 0.043 (3) | 0.002 (3) | −0.012 (3) | −0.003 (2) |
C16 | 0.035 (3) | 0.035 (3) | 0.030 (3) | 0.008 (2) | −0.007 (3) | −0.005 (2) |
C17 | 0.029 (3) | 0.027 (2) | 0.026 (2) | 0.004 (2) | −0.002 (2) | 0.0017 (18) |
Br1—C17 | 1.892 (5) | C6—H6A | 0.9500 |
O1—C12 | 1.386 (5) | C7—C8 | 1.395 (6) |
O1—C1 | 1.452 (5) | C7—H7A | 0.9500 |
O2—C2 | 1.433 (5) | C8—C9 | 1.458 (6) |
O2—H1O | 0.78 (6) | C9—C10 | 1.324 (6) |
C1—C10 | 1.504 (6) | C9—H9A | 0.9500 |
C1—C2 | 1.528 (5) | C10—H10A | 0.9500 |
C1—H1A | 1.0000 | C12—C17 | 1.383 (6) |
C2—C3 | 1.504 (6) | C12—C13 | 1.398 (6) |
C2—H2A | 1.0000 | C13—C14 | 1.388 (6) |
C3—C4 | 1.387 (6) | C13—H13A | 0.9500 |
C3—C8 | 1.413 (6) | C14—C15 | 1.387 (7) |
C4—C5 | 1.399 (6) | C14—H14A | 0.9500 |
C4—H4A | 0.9500 | C15—C16 | 1.383 (7) |
C5—C6 | 1.376 (6) | C15—H15A | 0.9500 |
C5—H5A | 0.9500 | C16—C17 | 1.391 (6) |
C6—C7 | 1.391 (6) | C16—H16A | 0.9500 |
C12—O1—C1 | 115.9 (4) | C8—C7—H7A | 119.5 |
C2—O2—H1O | 114 (5) | C7—C8—C3 | 118.9 (4) |
O1—C1—C10 | 110.5 (4) | C7—C8—C9 | 121.7 (4) |
O1—C1—C2 | 108.0 (4) | C3—C8—C9 | 119.4 (4) |
C10—C1—C2 | 110.3 (3) | C10—C9—C8 | 120.5 (4) |
O1—C1—H1A | 109.3 | C10—C9—H9A | 119.8 |
C10—C1—H1A | 109.3 | C8—C9—H9A | 119.8 |
C2—C1—H1A | 109.3 | C9—C10—C1 | 120.4 (4) |
O2—C2—C3 | 109.8 (3) | C9—C10—H10A | 119.8 |
O2—C2—C1 | 111.2 (3) | C1—C10—H10A | 119.8 |
C3—C2—C1 | 110.2 (4) | C17—C12—O1 | 120.1 (4) |
O2—C2—H2A | 108.5 | C17—C12—C13 | 119.6 (4) |
C3—C2—H2A | 108.5 | O1—C12—C13 | 120.2 (4) |
C1—C2—H2A | 108.5 | C14—C13—C12 | 119.3 (5) |
C4—C3—C8 | 119.5 (4) | C14—C13—H13A | 120.4 |
C4—C3—C2 | 122.4 (4) | C12—C13—H13A | 120.4 |
C8—C3—C2 | 118.1 (4) | C15—C14—C13 | 120.9 (5) |
C3—C4—C5 | 120.5 (4) | C15—C14—H14A | 119.6 |
C3—C4—H4A | 119.7 | C13—C14—H14A | 119.6 |
C5—C4—H4A | 119.7 | C16—C15—C14 | 119.6 (5) |
C6—C5—C4 | 120.3 (4) | C16—C15—H15A | 120.2 |
C6—C5—H5A | 119.9 | C14—C15—H15A | 120.2 |
C4—C5—H5A | 119.9 | C15—C16—C17 | 119.8 (5) |
C5—C6—C7 | 119.7 (4) | C15—C16—H16A | 120.1 |
C5—C6—H6A | 120.2 | C17—C16—H16A | 120.1 |
C7—C6—H6A | 120.2 | C12—C17—C16 | 120.7 (4) |
C6—C7—C8 | 121.1 (4) | C12—C17—Br1 | 120.2 (3) |
C6—C7—H7A | 119.5 | C16—C17—Br1 | 119.1 (4) |
C12—O1—C1—C10 | −94.9 (4) | C2—C3—C8—C9 | 1.1 (6) |
C12—O1—C1—C2 | 144.3 (4) | C7—C8—C9—C10 | −161.4 (5) |
O1—C1—C2—O2 | −65.6 (5) | C3—C8—C9—C10 | 17.9 (7) |
C10—C1—C2—O2 | 173.6 (4) | C8—C9—C10—C1 | 1.6 (7) |
O1—C1—C2—C3 | 172.4 (3) | O1—C1—C10—C9 | −156.1 (4) |
C10—C1—C2—C3 | 51.5 (5) | C2—C1—C10—C9 | −36.8 (6) |
O2—C2—C3—C4 | 22.5 (6) | C1—O1—C12—C17 | 120.4 (5) |
C1—C2—C3—C4 | 145.3 (4) | C1—O1—C12—C13 | −61.3 (5) |
O2—C2—C3—C8 | −158.4 (4) | C17—C12—C13—C14 | 0.3 (7) |
C1—C2—C3—C8 | −35.5 (5) | O1—C12—C13—C14 | −178.0 (4) |
C8—C3—C4—C5 | 1.0 (7) | C12—C13—C14—C15 | 2.2 (7) |
C2—C3—C4—C5 | −179.9 (4) | C13—C14—C15—C16 | −2.9 (8) |
C3—C4—C5—C6 | −1.0 (7) | C14—C15—C16—C17 | 1.0 (7) |
C4—C5—C6—C7 | 0.5 (7) | O1—C12—C17—C16 | 176.1 (4) |
C5—C6—C7—C8 | 0.0 (7) | C13—C12—C17—C16 | −2.2 (7) |
C6—C7—C8—C3 | −0.1 (7) | O1—C12—C17—Br1 | −6.2 (6) |
C6—C7—C8—C9 | 179.2 (4) | C13—C12—C17—Br1 | 175.5 (3) |
C4—C3—C8—C7 | −0.4 (7) | C15—C16—C17—C12 | 1.6 (7) |
C2—C3—C8—C7 | −179.6 (4) | C15—C16—C17—Br1 | −176.2 (4) |
C4—C3—C8—C9 | −179.7 (4) |
D—H···A | D—H | H···A | D···A | D—H···A |
O2—H1O···O2i | 0.78 (6) | 2.00 (6) | 2.766 (3) | 168 (7) |
Symmetry code: (i) x+1/2, −y+1/2, −z+1. |
Experimental details
Crystal data | |
Chemical formula | C16H13BrO2 |
Mr | 317.17 |
Crystal system, space group | Orthorhombic, P212121 |
Temperature (K) | 150 |
a, b, c (Å) | 4.6070 (2), 11.2898 (4), 24.9751 (12) |
V (Å3) | 1299.01 (10) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 3.16 |
Crystal size (mm) | 0.35 × 0.08 × 0.08 |
Data collection | |
Diffractometer | Nonius KappaCCD diffractometer |
Absorption correction | Multi-scan (DENZO-SMN; Otwinowski & Minor, 1997) |
Tmin, Tmax | 0.404, 0.786 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 6770, 2317, 1897 |
Rint | 0.085 |
(sin θ/λ)max (Å−1) | 0.595 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.039, 0.085, 1.02 |
No. of reflections | 2317 |
No. of parameters | 177 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.38, −0.40 |
Absolute structure | (Flack, 1983) |
Absolute structure parameter | 0.015 (16) |
Computer programs: COLLECT (Nonius, 1997-2001), DENZO-SMN (Otwinowski & Minor, 1997), DENZO-SMN, SHELXTL/PC (Sheldrick, 2001), SHELXTL/PC.
O1—C12 | 1.386 (5) | C1—C10 | 1.504 (6) |
O1—C1 | 1.452 (5) | C1—C2 | 1.528 (5) |
O2—C2 | 1.433 (5) | C2—C3 | 1.504 (6) |
C12—O1—C1 | 115.9 (4) | ||
C12—O1—C1—C2 | 144.3 (4) | C1—O1—C12—C13 | −61.3 (5) |
D—H···A | D—H | H···A | D···A | D—H···A |
O2—H1O···O2i | 0.78 (6) | 2.00 (6) | 2.766 (3) | 168 (7) |
Symmetry code: (i) x+1/2, −y+1/2, −z+1. |
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Recently, we reported a new rhodium-catalysed ring-opening reaction of 1,4-dihydro-1,4-epoxynaphthalene with a wide range of phenols (Lautens et al., 2000). The 1,2-regio-, trans and relative stereochemistry, as well as the absolute stereochemistry, for the addition of 2-bomophenol were established by X-ray diffraction analysis when (R)-(-)-1-[(S)-2-(diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine [(R)-(S)-PPF-PtBu2] is used as the chiral ligand.
Molecules of the title compound, (I), are linked through 21 screw axes to form intermolecular hydrogen-bonded chains parallel to the a axis (Fig. 2 and Table 2). In the dihydronaphthalene group, an analysis (Cremer & Pople, 1975) of the puckering in the six-membered ring (C1/C2/C3/C8/C9/C10) gives QT = 0.466 (4) Å. The conformation analysis of that ring (Duax et al., 1976) shows that the conformation is a half-chair, with a local pseudo-twofold axis running along the midpoints of the C1—C2 and C8—C9 bonds.