Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807017783/hb2363sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807017783/hb2363IIsup2.hkl |
CCDC reference: 647563
A commercial sample of 3-acetylaminobenzoic acid was used. Single crystals of (II) were grown from a water–methanol solution by vapour diffusion of water.
The crystals of (II) were of poor quality and weakly diffracting, which accounts for the low fraction of measured reflections. All H atoms, except for those attached to the C9 methyl group, were located in difference maps and their positions and Uiso values were refined freely. The C9 H atoms were positioned geometrically over two orientations of equal occupancy and refined as riding, with C—H = 0.95 Å and Uiso(H) = 1.2Ueq(C9).
The crystal structures of 2-acetylaminobenzoic acid, (I) (Kovalevsky, 1999; Mascarenhas et al., 1980; Rajnikant & Deshmukh, 2004), and 4-acetylaminobenzoic acid, (III) (Kashino et al., 1986; Feeder & Jones, 1992), have been described in the literature. The crystal structure of the title compound (II) has not been solved to date. Therefore, in the present work, we have attempted to fill this gap (Fig. 1, Table 1).
The dihedral angle in (II) between the mean plane of the aromatic ring and the plane of atoms C7/O3/O1 is 6.5 (3)°. The corresponding angle between the ring and the acetyl group C2/C1/N1/C8 is 6.3 (3)°.
The unit-cell packing of (II) is shown in Figs. 2 and 3. The molecules form layers held together by N—H···O and O—H···O hydrogen bonds. The layers interact with each other by van der Waals forces. The topology of the hydrogen-bond network of (II) can be described by the graph-set assignments introduced by Etter (1990) as a C(9) chain along the c axis and an R22(14) intermolecular ring. The hydrogen-bond networks in (I) and (III) can be characterized as S(6) and C(8), and C(4) and R22(8), respectively.
For the crystal structures of the ortho- and para-isomers of the title compound, see: Feeder & Jones (1992); Kashino et al. (1986); Kovalevsky (1999); Mascarenhas et al. (1980); Rajnikant & Deshmukh (2004).
For related literature, see: Etter (1990).
Data collection: CrystalClear (Rigaku, 2005); cell refinement: CrystalClear; data reduction: CrystalStructure (Rigaku, 2005); program(s) used to solve structure: SIR92 (Altomare et al., 1994); program(s) used to refine structure: CRYSTALS (Watkin et al., 1996); molecular graphics: CrystalStructure; software used to prepare material for publication: CrystalStructure.
C9H9NO3 | F(000) = 376.00 |
Mr = 179.17 | Dx = 1.422 Mg m−3 |
Monoclinic, P21/n | Mo Kα radiation, λ = 0.71070 Å |
Hall symbol: -P 2yn | Cell parameters from 1899 reflections |
a = 3.9522 (15) Å | θ = 2.8–30.5° |
b = 10.699 (4) Å | µ = 0.11 mm−1 |
c = 19.831 (7) Å | T = 293 K |
β = 93.393 (8)° | Prism, colourless |
V = 837.1 (5) Å3 | 0.60 × 0.10 × 0.05 mm |
Z = 4 |
Rigaku Saturn CCD area-detector diffractometer | 1168 reflections with F2 > 2σ(F2) |
Detector resolution: 7.31 pixels mm-1 | Rint = 0.031 |
ω scans | θmax = 32.0° |
Absorption correction: multi-scan (Jacobson, 1998) | h = −5→4 |
Tmin = 0.937, Tmax = 0.995 | k = −15→14 |
9339 measured reflections | l = −27→26 |
2325 independent reflections |
Refinement on F | Weighting scheme based on measured s.u.'s w = 1/σ2(Fo) |
R[F2 > 2σ(F2)] = 0.052 | (Δ/σ)max = 0.012 |
wR(F2) = 0.037 | Δρmax = 0.22 e Å−3 |
S = 1.50 | Δρmin = −0.17 e Å−3 |
1187 reflections | Extinction correction: Larson (1970), equation 22 |
152 parameters | Extinction coefficient: 50 (6) |
H atoms treated by a mixture of independent and constrained refinement |
C9H9NO3 | V = 837.1 (5) Å3 |
Mr = 179.17 | Z = 4 |
Monoclinic, P21/n | Mo Kα radiation |
a = 3.9522 (15) Å | µ = 0.11 mm−1 |
b = 10.699 (4) Å | T = 293 K |
c = 19.831 (7) Å | 0.60 × 0.10 × 0.05 mm |
β = 93.393 (8)° |
Rigaku Saturn CCD area-detector diffractometer | 2325 independent reflections |
Absorption correction: multi-scan (Jacobson, 1998) | 1168 reflections with F2 > 2σ(F2) |
Tmin = 0.937, Tmax = 0.995 | Rint = 0.031 |
9339 measured reflections |
R[F2 > 2σ(F2)] = 0.052 | 152 parameters |
wR(F2) = 0.037 | H atoms treated by a mixture of independent and constrained refinement |
S = 1.50 | Δρmax = 0.22 e Å−3 |
1187 reflections | Δρmin = −0.17 e Å−3 |
Refinement. Refinement using reflections with F2 > 2.0 σ(F2). The weighted R-factor(wR), goodness of fit (S) and R-factor (gt) are based on F, with F set to zero for negative F. The threshold expression of F2 > 2.0 σ(F2) is used only for calculating R-factor (gt). |
x | y | z | Uiso*/Ueq | Occ. (<1) | |
O1 | 0.4578 (5) | 0.19844 (17) | 0.24639 (8) | 0.0669 (6) | |
O2 | 0.9126 (4) | 0.11335 (16) | −0.10208 (8) | 0.0619 (6) | |
O3 | 0.7144 (5) | 0.30147 (17) | −0.12845 (10) | 0.0696 (7) | |
N1 | 0.6495 (5) | 0.09474 (19) | 0.15195 (10) | 0.0443 (6) | |
C1 | 0.5574 (5) | 0.1793 (2) | 0.10074 (11) | 0.0388 (7) | |
C2 | 0.6738 (6) | 0.1521 (2) | 0.03496 (12) | 0.0403 (7) | |
C3 | 0.6057 (5) | 0.2333 (2) | −0.01719 (11) | 0.0393 (7) | |
C4 | 0.4122 (6) | 0.3398 (2) | −0.00383 (12) | 0.0448 (8) | |
C5 | 0.2922 (6) | 0.3649 (2) | 0.06125 (13) | 0.0477 (8) | |
C6 | 0.3639 (6) | 0.2857 (2) | 0.11430 (12) | 0.0436 (7) | |
C7 | 0.7576 (6) | 0.2074 (2) | −0.08637 (12) | 0.0462 (8) | |
C8 | 0.5988 (6) | 0.1067 (2) | 0.21953 (12) | 0.0477 (8) | |
C9 | 0.7234 (6) | −0.0009 (2) | 0.25989 (12) | 0.0614 (9) | |
H1 | 0.780 (5) | 0.021 (2) | 0.1341 (11) | 0.077 (9)* | |
H2 | 0.822 (4) | 0.0766 (18) | 0.0236 (10) | 0.044 (6)* | |
H4 | 0.377 (5) | 0.396 (2) | −0.0423 (11) | 0.056 (7)* | |
H5 | 0.147 (5) | 0.4411 (19) | 0.0738 (10) | 0.055 (7)* | |
H6 | 0.272 (4) | 0.3037 (17) | 0.1606 (10) | 0.042 (6)* | |
H7 | 0.821 (7) | 0.286 (2) | −0.1736 (17) | 0.120 (11)* | |
H8 | 0.7098 | −0.0743 | 0.2329 | 0.073* | 0.50 |
H9 | 0.5888 | −0.0111 | 0.2976 | 0.073* | 0.50 |
H10 | 0.9525 | 0.0133 | 0.2752 | 0.073* | 0.50 |
H11 | 0.9227 | −0.0622 | 0.2293 | 0.073* | 0.50 |
H12 | 0.8177 | 0.0348 | 0.3013 | 0.073* | 0.50 |
H13 | 0.5133 | −0.0634 | 0.2731 | 0.073* | 0.50 |
U11 | U22 | U33 | U12 | U13 | U23 | |
O1 | 0.1056 (16) | 0.0619 (13) | 0.0334 (10) | 0.0159 (11) | 0.0067 (10) | −0.0059 (9) |
O2 | 0.0922 (14) | 0.0543 (12) | 0.0395 (11) | 0.0146 (11) | 0.0056 (9) | −0.0051 (9) |
O3 | 0.1094 (17) | 0.0633 (14) | 0.0367 (11) | 0.0188 (11) | 0.0093 (11) | 0.0114 (10) |
N1 | 0.0594 (13) | 0.0427 (13) | 0.0305 (11) | 0.0021 (11) | 0.0009 (9) | −0.0005 (10) |
C1 | 0.0475 (15) | 0.0381 (14) | 0.0305 (13) | −0.0041 (12) | 0.0005 (11) | 0.0006 (11) |
C2 | 0.0507 (15) | 0.0382 (14) | 0.0320 (14) | 0.0001 (13) | 0.0012 (11) | −0.0035 (12) |
C3 | 0.0471 (14) | 0.0395 (14) | 0.0308 (14) | −0.0066 (12) | −0.0006 (11) | −0.0008 (12) |
C4 | 0.0528 (17) | 0.0443 (16) | 0.0367 (15) | −0.0042 (13) | −0.0024 (13) | 0.0028 (13) |
C5 | 0.0507 (16) | 0.0421 (16) | 0.0502 (17) | 0.0055 (13) | 0.0027 (13) | −0.0021 (14) |
C6 | 0.0527 (16) | 0.0437 (15) | 0.0347 (14) | 0.0001 (13) | 0.0052 (12) | −0.0052 (13) |
C7 | 0.0576 (17) | 0.0468 (16) | 0.0334 (15) | −0.0053 (14) | −0.0042 (12) | 0.0007 (13) |
C8 | 0.0571 (17) | 0.0521 (17) | 0.0339 (15) | −0.0091 (14) | 0.0027 (12) | 0.0007 (14) |
C9 | 0.079 (2) | 0.0635 (19) | 0.0407 (17) | 0.0043 (16) | −0.0060 (15) | 0.0121 (15) |
O1—C8 | 1.262 (3) | C5—C6 | 1.368 (3) |
O2—C7 | 1.228 (3) | C8—C9 | 1.471 (3) |
O3—C7 | 1.312 (3) | O3—H7 | 1.02 (3) |
N1—C1 | 1.392 (2) | N1—H1 | 1.02 (2) |
N1—C8 | 1.373 (3) | C2—H2 | 1.031 (19) |
C1—C2 | 1.438 (3) | C4—H4 | 0.97 (2) |
C1—C6 | 1.406 (3) | C5—H5 | 1.04 (2) |
C2—C3 | 1.365 (3) | C6—H6 | 1.03 (2) |
C3—C4 | 1.406 (3) | C9—H8 | 0.950 |
C3—C7 | 1.555 (3) | C9—H9 | 0.950 |
C4—C5 | 1.427 (3) | C9—H10 | 0.950 |
C1—N1—C8 | 127.2 (2) | C1—C2—H2 | 125.0 (11) |
N1—C1—C2 | 116.5 (2) | C3—C2—H2 | 115.0 (11) |
N1—C1—C6 | 120.5 (2) | C3—C4—H4 | 113.8 (13) |
C2—C1—C6 | 122.9 (2) | C5—C4—H4 | 123.7 (13) |
C1—C2—C3 | 120.0 (2) | C4—C5—H5 | 125.8 (12) |
C2—C3—C4 | 117.2 (2) | C6—C5—H5 | 113.3 (12) |
C2—C3—C7 | 119.1 (2) | C1—C6—H6 | 123.2 (10) |
C4—C3—C7 | 123.6 (2) | C5—C6—H6 | 120.3 (10) |
C3—C4—C5 | 122.5 (2) | C8—C9—H8 | 109.6 |
C4—C5—C6 | 120.9 (2) | C8—C9—H9 | 109.5 |
C1—C6—C5 | 116.4 (2) | C8—C9—H10 | 109.4 |
O2—C7—O3 | 121.0 (2) | C8—C9—H11 | 110.9 |
O2—C7—C3 | 126.5 (2) | C8—C9—H12 | 104.7 |
O3—C7—C3 | 112.5 (2) | C8—C9—H13 | 111.7 |
O1—C8—N1 | 125.3 (2) | H8—C9—H9 | 109.5 |
O1—C8—C9 | 121.4 (2) | H8—C9—H10 | 109.5 |
N1—C8—C9 | 113.2 (2) | H9—C9—H10 | 109.5 |
C7—O3—H7 | 112.8 (16) | H11—C9—H12 | 114.3 |
C1—N1—H1 | 111.4 (13) | H11—C9—H13 | 108.0 |
C8—N1—H1 | 121.3 (13) | H12—C9—H13 | 107.2 |
C1—N1—C8—O1 | −0.1 (2) | C1—C2—C3—C7 | 175.3 (2) |
C1—N1—C8—C9 | 179.2 (2) | C2—C3—C4—C5 | 0.7 (3) |
C8—N1—C1—C2 | 172.9 (2) | C2—C3—C7—O2 | 7.3 (3) |
C8—N1—C1—C6 | −6.3 (3) | C2—C3—C7—O3 | −170.5 (2) |
N1—C1—C2—C3 | −177.3 (2) | C4—C3—C7—O2 | −175.8 (2) |
N1—C1—C6—C5 | 178.5 (2) | C4—C3—C7—O3 | 6.4 (3) |
C2—C1—C6—C5 | −0.7 (3) | C7—C3—C4—C5 | −176.3 (2) |
C6—C1—C2—C3 | 1.9 (3) | C3—C4—C5—C6 | 0.5 (3) |
C1—C2—C3—C4 | −1.8 (3) | C4—C5—C6—C1 | −0.5 (3) |
D—H···A | D—H | H···A | D···A | D—H···A |
O3—H7···O1i | 1.02 (3) | 1.71 (3) | 2.714 (2) | 164 (2) |
N1—H1···O2ii | 1.02 (2) | 2.01 (2) | 3.022 (2) | 173.3 (18) |
Symmetry codes: (i) x+1/2, −y+1/2, z−1/2; (ii) −x+2, −y, −z. |
Experimental details
Crystal data | |
Chemical formula | C9H9NO3 |
Mr | 179.17 |
Crystal system, space group | Monoclinic, P21/n |
Temperature (K) | 293 |
a, b, c (Å) | 3.9522 (15), 10.699 (4), 19.831 (7) |
β (°) | 93.393 (8) |
V (Å3) | 837.1 (5) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 0.11 |
Crystal size (mm) | 0.60 × 0.10 × 0.05 |
Data collection | |
Diffractometer | Rigaku Saturn CCD area-detector |
Absorption correction | Multi-scan (Jacobson, 1998) |
Tmin, Tmax | 0.937, 0.995 |
No. of measured, independent and observed [F2 > 2σ(F2)] reflections | 9339, 2325, 1168 |
Rint | 0.031 |
(sin θ/λ)max (Å−1) | 0.745 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.052, 0.037, 1.50 |
No. of reflections | 1187 |
No. of parameters | 152 |
No. of restraints | ? |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.22, −0.17 |
Computer programs: CrystalClear (Rigaku, 2005), CrystalClear, CrystalStructure (Rigaku, 2005), SIR92 (Altomare et al., 1994), CRYSTALS (Watkin et al., 1996), CrystalStructure.
D—H···A | D—H | H···A | D···A | D—H···A |
O3—H7···O1i | 1.02 (3) | 1.71 (3) | 2.714 (2) | 164 (2) |
N1—H1···O2ii | 1.02 (2) | 2.01 (2) | 3.022 (2) | 173.3 (18) |
Symmetry codes: (i) x+1/2, −y+1/2, z−1/2; (ii) −x+2, −y, −z. |
The crystal structures of 2-acetylaminobenzoic acid, (I) (Kovalevsky, 1999; Mascarenhas et al., 1980; Rajnikant & Deshmukh, 2004), and 4-acetylaminobenzoic acid, (III) (Kashino et al., 1986; Feeder & Jones, 1992), have been described in the literature. The crystal structure of the title compound (II) has not been solved to date. Therefore, in the present work, we have attempted to fill this gap (Fig. 1, Table 1).
The dihedral angle in (II) between the mean plane of the aromatic ring and the plane of atoms C7/O3/O1 is 6.5 (3)°. The corresponding angle between the ring and the acetyl group C2/C1/N1/C8 is 6.3 (3)°.
The unit-cell packing of (II) is shown in Figs. 2 and 3. The molecules form layers held together by N—H···O and O—H···O hydrogen bonds. The layers interact with each other by van der Waals forces. The topology of the hydrogen-bond network of (II) can be described by the graph-set assignments introduced by Etter (1990) as a C(9) chain along the c axis and an R22(14) intermolecular ring. The hydrogen-bond networks in (I) and (III) can be characterized as S(6) and C(8), and C(4) and R22(8), respectively.