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organic compounds
2,2,2-Trichloro-N-(3-nitrophenyl)acetamide
aPhysics Department, Manipal Institute of Technology, Manipal University, Manipal 576 104, India, bSolid State and Sructural Chemistry Unit, Indian Institute of Science, Bangalore 560 012, India, and cDepartment of Chemistry, Mangalore University 575 199, Karnataka, India
*Correspondence e-mail: v.upadhyaya@manipal.edu
In the title compound, C8H5Cl3N2O3, the dihedral angle between the nitrophenyl ring and the acetamide group is 5.47 (6)°. In the crystal, N—H⋯O and C—H⋯O hydrogen bonds link the molecules into chains running parallel to the b axis.
Related literature
For background to acetamides, see: Khan et al. (2010); Tahir & Shad (2011
). For a related structure, see: Rosli et al. (2007
). For hydrogen-bond motifs, see: Bernstein et al. (1995
).
Experimental
Crystal data
|
Refinement
|
|
Data collection: SMART (Bruker, 1998); cell SAINT-Plus (Bruker, 1998
) (Bruker, 1998
); data reduction: SAINT-Plus; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008
); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008
); molecular graphics: ORTEP-3 (Farrugia, 1997
) and CAMERON (Watkin et al., 1993
); software used to prepare material for publication: WinGX (Farrugia, 1999
).
Supporting information
https://doi.org/10.1107/S1600536812036732/pv2576sup1.cif
contains datablocks global, I. DOI:Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536812036732/pv2576Isup2.hkl
Supporting information file. DOI: https://doi.org/10.1107/S1600536812036732/pv2576Isup3.cml
3-Nitroaniline (1.0 g, 0.0072 mmol) was dissolved in 2M hydrochloric acid (5.0 ml), and added a little crushed ice. A solution of hydrated sodium acetate (5.0 g) in 25 ml of water was introduced, followed by trichloroacetic anhydride (4.5 g, 0.01457 mol). The mixture was shaken in the cold until the smell of trichloroacetic anhydride disappeared. The title compound was collected by filtration and recrystallized from an aqueous ethanol (75%) solution; yield: 1.52 g (75%), m.p. 376.15–378.15 K.
The H atoms were placed at calculated positions in the riding model approximation with N—H = 0.86 and C—H = 0.93 Å, and Uiso(H) = 1.2Ueq(N/C).
In view of earlier studies and interest owing to the biological activity of acetamide (Khan et al., 2010; Tahir & Shad, 2011), we report herein the
of the title compound. In the title compound, the nitro phenyl ring makes a dihedral angle of 5.47 (6)° with acetamide group. Bond lengths and angles are within the normal ranges and are comparable with a related structure (Rosli et al., 2007). In the crystal, an S(6) ring motif (Bernstein et al., 1995) is formed via intramolecular C8—H8A···O1 hydrogen bond (Table 1). The C—H···O and C—H···N hydrogen bonding intractions (Table 1 and Figure 2) result in bifurcated bonds and link the molecules into chains along the b-axis.For background to acetamides, see: Khan et al. (2010); Tahir & Shad (2011). For a related structure, see: Rosli et al. (2007). For hydrogen-bond motifs, see: Bernstein et al. (1995).
Data collection: SMART (Bruker, 1998); cell
SAINT-Plus (Bruker, 1998); data reduction: SAINT-Plus (Bruker, 1998); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 (Farrugia, 1997) and CAMERON (Watkin et al., 1993); software used to prepare material for publication: WinGX (Farrugia, 1999).C8H5Cl3N2O3 | F(000) = 1136 |
Mr = 283.49 | Dx = 1.620 Mg m−3 |
Orthorhombic, Pbca | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: -P 2ac 2ab | Cell parameters from 2532 reflections |
a = 11.5164 (8) Å | θ = 2.1–27.0° |
b = 10.1427 (5) Å | µ = 0.78 mm−1 |
c = 19.9054 (11) Å | T = 296 K |
V = 2325.1 (2) Å3 | Block, yellow |
Z = 8 | 0.20 × 0.18 × 0.18 mm |
Bruker SMART APEX CCD detector diffractometer | 2532 independent reflections |
Radiation source: Enhance (Mo) X-ray Source | 1713 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.028 |
ω scans | θmax = 27.0°, θmin = 2.1° |
Absorption correction: multi-scan (SAINT-Plus; Bruker, 1998) | h = −5→14 |
Tmin = 0.860, Tmax = 0.872 | k = −10→12 |
8739 measured reflections | l = −14→25 |
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)] = 0.049 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.144 | H-atom parameters constrained |
S = 1.07 | w = 1/[σ2(Fo2) + (0.0695P)2 + 0.9222P] where P = (Fo2 + 2Fc2)/3 |
2532 reflections | (Δ/σ)max = 0.001 |
145 parameters | Δρmax = 0.46 e Å−3 |
0 restraints | Δρmin = −0.37 e Å−3 |
C8H5Cl3N2O3 | V = 2325.1 (2) Å3 |
Mr = 283.49 | Z = 8 |
Orthorhombic, Pbca | Mo Kα radiation |
a = 11.5164 (8) Å | µ = 0.78 mm−1 |
b = 10.1427 (5) Å | T = 296 K |
c = 19.9054 (11) Å | 0.20 × 0.18 × 0.18 mm |
Bruker SMART APEX CCD detector diffractometer | 2532 independent reflections |
Absorption correction: multi-scan (SAINT-Plus; Bruker, 1998) | 1713 reflections with I > 2σ(I) |
Tmin = 0.860, Tmax = 0.872 | Rint = 0.028 |
8739 measured reflections |
R[F2 > 2σ(F2)] = 0.049 | 0 restraints |
wR(F2) = 0.144 | H-atom parameters constrained |
S = 1.07 | Δρmax = 0.46 e Å−3 |
2532 reflections | Δρmin = −0.37 e Å−3 |
145 parameters |
Geometry. All s.u.'s (except the s.u. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell s.u.'s are taken into account individually in the estimation of s.u.'s in distances, angles and torsion angles; correlations between s.u.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell s.u.'s is used for estimating s.u.'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 > 2σ(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 | ||
C1 | 0.8599 (3) | 0.8973 (3) | 0.29007 (15) | 0.0522 (8) | |
C2 | 0.7513 (2) | 0.9294 (2) | 0.33324 (13) | 0.0390 (6) | |
C3 | 0.5939 (2) | 0.8197 (2) | 0.39617 (13) | 0.0367 (6) | |
C4 | 0.5685 (3) | 0.7018 (3) | 0.42914 (16) | 0.0520 (7) | |
H4 | 0.6196 | 0.6310 | 0.4260 | 0.062* | |
C5 | 0.4687 (3) | 0.6897 (3) | 0.4662 (2) | 0.0705 (10) | |
H5 | 0.4522 | 0.6103 | 0.4876 | 0.085* | |
C6 | 0.3927 (3) | 0.7935 (3) | 0.47228 (18) | 0.0621 (9) | |
H6 | 0.3243 | 0.7852 | 0.4968 | 0.074* | |
C7 | 0.4209 (2) | 0.9099 (3) | 0.44096 (14) | 0.0429 (6) | |
C8 | 0.5197 (2) | 0.9263 (2) | 0.40254 (13) | 0.0387 (6) | |
H8A | 0.5358 | 1.0063 | 0.3817 | 0.046* | |
Cl1 | 0.82157 (11) | 0.79451 (9) | 0.22201 (5) | 0.0843 (4) | |
Cl3 | 0.92258 (9) | 1.04369 (8) | 0.25994 (5) | 0.0801 (4) | |
Cl2 | 0.96357 (8) | 0.81360 (10) | 0.34058 (6) | 0.0828 (3) | |
N1 | 0.3404 (2) | 1.0223 (3) | 0.44728 (15) | 0.0580 (7) | |
N2 | 0.6956 (2) | 0.82155 (19) | 0.35614 (12) | 0.0433 (6) | |
H2N | 0.7247 | 0.7464 | 0.3454 | 0.052* | |
O1 | 0.72365 (18) | 1.04229 (16) | 0.34446 (11) | 0.0524 (5) | |
O2 | 0.3623 (2) | 1.1225 (2) | 0.41711 (16) | 0.0858 (8) | |
O3 | 0.2570 (2) | 1.0101 (3) | 0.48485 (16) | 0.0900 (9) |
U11 | U22 | U33 | U12 | U13 | U23 | |
C1 | 0.0626 (19) | 0.0350 (14) | 0.0589 (18) | −0.0020 (13) | 0.0223 (15) | 0.0010 (12) |
C2 | 0.0444 (14) | 0.0307 (12) | 0.0418 (14) | −0.0010 (11) | 0.0055 (13) | 0.0007 (10) |
C3 | 0.0383 (14) | 0.0318 (12) | 0.0400 (13) | −0.0053 (10) | −0.0002 (12) | −0.0019 (10) |
C4 | 0.0499 (17) | 0.0353 (14) | 0.071 (2) | 0.0007 (12) | 0.0134 (16) | 0.0083 (13) |
C5 | 0.064 (2) | 0.0461 (18) | 0.101 (3) | −0.0008 (15) | 0.027 (2) | 0.0226 (17) |
C6 | 0.0453 (17) | 0.0588 (19) | 0.082 (2) | −0.0057 (14) | 0.0193 (17) | 0.0078 (16) |
C7 | 0.0368 (14) | 0.0433 (14) | 0.0485 (15) | 0.0011 (11) | −0.0027 (13) | −0.0063 (12) |
C8 | 0.0412 (14) | 0.0332 (13) | 0.0416 (14) | −0.0015 (10) | −0.0005 (12) | −0.0017 (10) |
Cl1 | 0.1194 (9) | 0.0689 (6) | 0.0645 (6) | −0.0233 (5) | 0.0383 (6) | −0.0211 (4) |
Cl3 | 0.0991 (8) | 0.0439 (4) | 0.0973 (7) | −0.0162 (4) | 0.0522 (6) | 0.0022 (4) |
Cl2 | 0.0527 (5) | 0.0816 (6) | 0.1141 (8) | 0.0127 (4) | 0.0146 (5) | 0.0168 (6) |
N1 | 0.0462 (15) | 0.0550 (16) | 0.0728 (18) | 0.0068 (12) | 0.0062 (14) | −0.0033 (13) |
N2 | 0.0482 (13) | 0.0234 (10) | 0.0584 (14) | 0.0020 (9) | 0.0148 (11) | 0.0000 (9) |
O1 | 0.0560 (12) | 0.0243 (9) | 0.0767 (14) | −0.0014 (8) | 0.0169 (11) | −0.0020 (8) |
O2 | 0.0786 (18) | 0.0568 (15) | 0.122 (2) | 0.0245 (13) | 0.0300 (16) | 0.0152 (15) |
O3 | 0.0544 (15) | 0.0901 (18) | 0.125 (2) | 0.0202 (13) | 0.0345 (16) | 0.0105 (17) |
C1—C2 | 1.552 (4) | C5—C6 | 1.374 (4) |
C1—Cl3 | 1.756 (3) | C5—H5 | 0.9300 |
C1—Cl1 | 1.766 (3) | C6—C7 | 1.374 (4) |
C1—Cl2 | 1.777 (3) | C6—H6 | 0.9300 |
C2—O1 | 1.209 (3) | C7—C8 | 1.380 (4) |
C2—N2 | 1.348 (3) | C7—N1 | 1.476 (4) |
C3—C8 | 1.385 (3) | C8—H8A | 0.9300 |
C3—C4 | 1.395 (3) | N1—O2 | 1.207 (3) |
C3—N2 | 1.417 (3) | N1—O3 | 1.223 (4) |
C4—C5 | 1.372 (4) | N2—H2N | 0.8600 |
C4—H4 | 0.9300 | ||
C2—C1—Cl3 | 110.05 (18) | C6—C5—H5 | 119.6 |
C2—C1—Cl1 | 110.3 (2) | C7—C6—C5 | 117.9 (3) |
Cl3—C1—Cl1 | 109.88 (16) | C7—C6—H6 | 121.1 |
C2—C1—Cl2 | 109.17 (19) | C5—C6—H6 | 121.1 |
Cl3—C1—Cl2 | 108.75 (18) | C6—C7—C8 | 123.4 (3) |
Cl1—C1—Cl2 | 108.65 (15) | C6—C7—N1 | 118.5 (3) |
O1—C2—N2 | 125.5 (2) | C8—C7—N1 | 118.1 (2) |
O1—C2—C1 | 120.9 (2) | C7—C8—C3 | 117.7 (2) |
N2—C2—C1 | 113.6 (2) | C7—C8—H8A | 121.1 |
C8—C3—C4 | 119.8 (2) | C3—C8—H8A | 121.1 |
C8—C3—N2 | 123.5 (2) | O2—N1—O3 | 123.6 (3) |
C4—C3—N2 | 116.7 (2) | O2—N1—C7 | 118.5 (3) |
C5—C4—C3 | 120.4 (3) | O3—N1—C7 | 117.8 (3) |
C5—C4—H4 | 119.8 | C2—N2—C3 | 126.5 (2) |
C3—C4—H4 | 119.8 | C2—N2—H2N | 116.8 |
C4—C5—C6 | 120.8 (3) | C3—N2—H2N | 116.8 |
C4—C5—H5 | 119.6 | ||
Cl3—C1—C2—O1 | −3.2 (4) | C6—C7—C8—C3 | −0.6 (4) |
Cl1—C1—C2—O1 | −124.6 (3) | N1—C7—C8—C3 | −179.1 (2) |
Cl2—C1—C2—O1 | 116.1 (3) | C4—C3—C8—C7 | −1.2 (4) |
Cl3—C1—C2—N2 | 177.6 (2) | N2—C3—C8—C7 | 177.4 (2) |
Cl1—C1—C2—N2 | 56.2 (3) | C6—C7—N1—O2 | −176.5 (3) |
Cl2—C1—C2—N2 | −63.1 (3) | C8—C7—N1—O2 | 2.1 (4) |
C8—C3—C4—C5 | 1.9 (5) | C6—C7—N1—O3 | 6.1 (4) |
N2—C3—C4—C5 | −176.8 (3) | C8—C7—N1—O3 | −175.3 (3) |
C3—C4—C5—C6 | −0.8 (6) | O1—C2—N2—C3 | 1.3 (5) |
C4—C5—C6—C7 | −1.0 (6) | C1—C2—N2—C3 | −179.5 (3) |
C5—C6—C7—C8 | 1.8 (5) | C8—C3—N2—C2 | 18.2 (4) |
C5—C6—C7—N1 | −179.7 (3) | C4—C3—N2—C2 | −163.2 (3) |
D—H···A | D—H | H···A | D···A | D—H···A |
C8—H8A···O1 | 0.93 | 2.32 | 2.870 (3) | 117 |
C4—H4···O1i | 0.93 | 2.59 | 3.345 (4) | 138 |
N2—H2N···O1i | 0.86 | 2.15 | 2.990 (3) | 164 |
Symmetry code: (i) −x+3/2, y−1/2, z. |
Experimental details
Crystal data | |
Chemical formula | C8H5Cl3N2O3 |
Mr | 283.49 |
Crystal system, space group | Orthorhombic, Pbca |
Temperature (K) | 296 |
a, b, c (Å) | 11.5164 (8), 10.1427 (5), 19.9054 (11) |
V (Å3) | 2325.1 (2) |
Z | 8 |
Radiation type | Mo Kα |
µ (mm−1) | 0.78 |
Crystal size (mm) | 0.20 × 0.18 × 0.18 |
Data collection | |
Diffractometer | Bruker SMART APEX CCD detector |
Absorption correction | Multi-scan (SAINT-Plus; Bruker, 1998) |
Tmin, Tmax | 0.860, 0.872 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 8739, 2532, 1713 |
Rint | 0.028 |
(sin θ/λ)max (Å−1) | 0.639 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.049, 0.144, 1.07 |
No. of reflections | 2532 |
No. of parameters | 145 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.46, −0.37 |
Computer programs: SMART (Bruker, 1998), SAINT-Plus (Bruker, 1998), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 (Farrugia, 1997) and CAMERON (Watkin et al., 1993), WinGX (Farrugia, 1999).
D—H···A | D—H | H···A | D···A | D—H···A |
C4—H4···O1i | 0.930 | 2.589 | 3.345 (4) | 138 |
N2—H2N···O1i | 0.860 | 2.154 | 2.990 (3) | 164 |
Symmetry code: (i) −x+3/2, y−1/2, z. |
Acknowledgements
ANP is thankful to Manipal Institute of Technology, Manipal University and Mohamed Ziaulla, Bangalore University.
References
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In view of earlier studies and interest owing to the biological activity of acetamide (Khan et al., 2010; Tahir & Shad, 2011), we report herein the crystal structure of the title compound. In the title compound, the nitro phenyl ring makes a dihedral angle of 5.47 (6)° with acetamide group. Bond lengths and angles are within the normal ranges and are comparable with a related structure (Rosli et al., 2007). In the crystal, an S(6) ring motif (Bernstein et al., 1995) is formed via intramolecular C8—H8A···O1 hydrogen bond (Table 1). The C—H···O and C—H···N hydrogen bonding intractions (Table 1 and Figure 2) result in bifurcated bonds and link the molecules into chains along the b-axis.