organic compounds
3-(3,5-Dichloroanilinocarbonyl)propionic acid
aDepartment of Chemistry, Quaid-i-Azam University, Islamabad 45320, Pakistan, bUniversity of Sargodha, Department of Physics, Sagrodha, Pakistan, and cGovernment College University, Department of Chemistry, Lahore, Pakistan
*Correspondence e-mail: dmntahir_uos@yahoo.com
The 10H9Cl2NO3, consists of dimers due to intermolecular O—H⋯O hydrogen bonding forming an R22(8) ring through the carboxyl groups. These dimers are linked to each other by intermolecular hydrogen bonds between the amine group and the adjacent carbonyl O atom. A single C—Cl⋯π interaction is also observed between the chloro-substituted aromatic rings.
of the title compound, CExperimental
Crystal data
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Refinement
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Data collection: APEX2 (Bruker, 2007); cell APEX2; data reduction: SAINT (Bruker, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997) and PLATON (Spek, 2003); software used to prepare material for publication: WinGX (Farrugia, 1999) and PLATON.
Supporting information
10.1107/S1600536808008556/fj2109sup1.cif
contains datablocks global, I. DOI:Structure factors: contains datablock I. DOI: 10.1107/S1600536808008556/fj2109Isup2.hkl
3,5-Dichloroaniline (16.2 g, 0.1 mole) and succinic anhydride (10 g, 0.1 mole) were dissolved in glacial acetic acid separately and mixed. The mixed solution was stirred at room temperature for 24 h. The precipitated material was filtered, washed with distilled water and dried at 413–423 K. The title compound (I) was obtained by recrystallizing the dried product using aceton. (Yield: 90%, m.p. 437 K).
Data collection: APEX2 (Bruker, 2007); cell
APEX2 (Bruker, 2007); data reduction: SAINT (Bruker, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997) and PLATON (Spek, 2003); software used to prepare material for publication: WinGX (Farrugia, 1999) and PLATON (Spek, 2003).C10H9Cl2NO3 | Z = 2 |
Mr = 262.08 | F(000) = 268 |
Triclinic, P1 | Dx = 1.571 Mg m−3 |
Hall symbol: -P 1 | Mo Kα radiation, λ = 0.71073 Å |
a = 4.8568 (2) Å | Cell parameters from 2971 reflections |
b = 8.6677 (4) Å | θ = 1.5–29.2° |
c = 13.9038 (8) Å | µ = 0.58 mm−1 |
α = 74.467 (3)° | T = 296 K |
β = 80.495 (2)° | Needle, colourless |
γ = 82.712 (3)° | 0.25 × 0.12 × 0.10 mm |
V = 554.09 (5) Å3 |
Bruker KappaAPEXII CCD diffractometer | 2971 independent reflections |
Radiation source: fine-focus sealed tube | 2065 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.027 |
Detector resolution: 7.4 pixels mm-1 | θmax = 29.2°, θmin = 1.5° |
ω scans | h = −6→6 |
Absorption correction: multi-scan (SADABS; Bruker, 2005) | k = −11→11 |
Tmin = 0.870, Tmax = 0.945 | l = −19→18 |
12157 measured reflections |
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)] = 0.040 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.125 | Only H-atom coordinates refined |
S = 1.07 | w = 1/[σ2(Fo2) + (0.0492P)2 + 0.2158P] where P = (Fo2 + 2Fc2)/3 |
2971 reflections | (Δ/σ)max = 0.001 |
172 parameters | Δρmax = 0.27 e Å−3 |
0 restraints | Δρmin = −0.43 e Å−3 |
C10H9Cl2NO3 | γ = 82.712 (3)° |
Mr = 262.08 | V = 554.09 (5) Å3 |
Triclinic, P1 | Z = 2 |
a = 4.8568 (2) Å | Mo Kα radiation |
b = 8.6677 (4) Å | µ = 0.58 mm−1 |
c = 13.9038 (8) Å | T = 296 K |
α = 74.467 (3)° | 0.25 × 0.12 × 0.10 mm |
β = 80.495 (2)° |
Bruker KappaAPEXII CCD diffractometer | 2971 independent reflections |
Absorption correction: multi-scan (SADABS; Bruker, 2005) | 2065 reflections with I > 2σ(I) |
Tmin = 0.870, Tmax = 0.945 | Rint = 0.027 |
12157 measured reflections |
R[F2 > 2σ(F2)] = 0.040 | 0 restraints |
wR(F2) = 0.125 | Only H-atom coordinates refined |
S = 1.07 | Δρmax = 0.27 e Å−3 |
2971 reflections | Δρmin = −0.43 e Å−3 |
172 parameters |
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 | ||
Cl1 | −0.50817 (12) | 1.03658 (7) | 0.31192 (6) | 0.0754 (2) | |
Cl2 | 0.18783 (13) | 0.70434 (7) | 0.57110 (5) | 0.0704 (2) | |
O1 | 0.1715 (4) | 0.0213 (3) | 0.07439 (17) | 0.0910 (7) | |
H1 | 0.281 (8) | −0.046 (4) | 0.039 (3) | 0.109* | |
O2 | 0.5114 (3) | 0.1840 (3) | 0.01798 (15) | 0.0829 (6) | |
O3 | −0.1931 (3) | 0.5285 (3) | 0.18654 (16) | 0.0814 (6) | |
N1 | 0.2023 (3) | 0.5827 (3) | 0.23147 (16) | 0.0607 (5) | |
H1A | 0.377 (6) | 0.563 (3) | 0.222 (2) | 0.073* | |
C1 | 0.2819 (4) | 0.1536 (4) | 0.06543 (17) | 0.0629 (7) | |
C2 | 0.1014 (4) | 0.2656 (4) | 0.1188 (2) | 0.0636 (7) | |
H2A | −0.054 (6) | 0.295 (3) | 0.089 (2) | 0.076* | |
H2B | 0.031 (6) | 0.202 (3) | 0.186 (2) | 0.076* | |
C3 | 0.2413 (4) | 0.4095 (4) | 0.1194 (2) | 0.0653 (7) | |
H3A | 0.413 (6) | 0.381 (3) | 0.139 (2) | 0.078* | |
H3B | 0.275 (6) | 0.480 (3) | 0.051 (2) | 0.078* | |
C4 | 0.0626 (4) | 0.5118 (3) | 0.18182 (18) | 0.0588 (6) | |
C5 | 0.0789 (4) | 0.6763 (3) | 0.29919 (18) | 0.0525 (5) | |
C6 | −0.1369 (4) | 0.7959 (3) | 0.2744 (2) | 0.0558 (5) | |
H6 | −0.196 (5) | 0.813 (3) | 0.208 (2) | 0.067* | |
C7 | −0.2454 (4) | 0.8838 (2) | 0.3433 (2) | 0.0556 (6) | |
C8 | −0.1529 (4) | 0.8582 (2) | 0.4348 (2) | 0.0565 (6) | |
H8 | −0.234 (6) | 0.918 (3) | 0.4805 (19) | 0.068* | |
C9 | 0.0627 (4) | 0.7390 (2) | 0.45673 (19) | 0.0529 (5) | |
C10 | 0.1799 (4) | 0.6482 (2) | 0.39000 (19) | 0.0534 (5) | |
H10 | 0.323 (5) | 0.569 (3) | 0.4041 (18) | 0.064* |
U11 | U22 | U33 | U12 | U13 | U23 | |
Cl1 | 0.0467 (3) | 0.0511 (3) | 0.1229 (6) | 0.0104 (2) | −0.0224 (3) | −0.0129 (3) |
Cl2 | 0.0688 (4) | 0.0548 (3) | 0.0942 (5) | −0.0021 (3) | −0.0275 (3) | −0.0220 (3) |
O1 | 0.0561 (10) | 0.1287 (19) | 0.1042 (16) | −0.0241 (11) | 0.0243 (10) | −0.0704 (14) |
O2 | 0.0471 (9) | 0.1186 (16) | 0.0902 (13) | −0.0130 (9) | 0.0204 (9) | −0.0543 (12) |
O3 | 0.0227 (6) | 0.1166 (16) | 0.1185 (15) | 0.0053 (8) | −0.0064 (8) | −0.0601 (13) |
N1 | 0.0212 (7) | 0.0772 (13) | 0.0841 (14) | 0.0006 (7) | −0.0002 (7) | −0.0273 (11) |
C1 | 0.0344 (9) | 0.110 (2) | 0.0533 (13) | −0.0055 (11) | −0.0032 (9) | −0.0381 (13) |
C2 | 0.0293 (9) | 0.104 (2) | 0.0631 (15) | −0.0026 (10) | −0.0004 (9) | −0.0360 (14) |
C3 | 0.0273 (9) | 0.0925 (19) | 0.0749 (16) | 0.0001 (10) | 0.0053 (9) | −0.0290 (14) |
C4 | 0.0240 (8) | 0.0786 (15) | 0.0716 (15) | −0.0001 (8) | −0.0007 (8) | −0.0208 (12) |
C5 | 0.0242 (7) | 0.0512 (11) | 0.0789 (15) | −0.0053 (7) | 0.0001 (8) | −0.0146 (10) |
C6 | 0.0306 (8) | 0.0564 (13) | 0.0747 (15) | −0.0046 (8) | −0.0058 (9) | −0.0074 (11) |
C7 | 0.0301 (8) | 0.0381 (10) | 0.0934 (17) | −0.0015 (7) | −0.0078 (9) | −0.0086 (10) |
C8 | 0.0404 (10) | 0.0379 (11) | 0.0926 (18) | −0.0046 (8) | −0.0083 (10) | −0.0187 (11) |
C9 | 0.0406 (9) | 0.0367 (10) | 0.0822 (15) | −0.0072 (8) | −0.0133 (9) | −0.0118 (10) |
C10 | 0.0337 (9) | 0.0388 (10) | 0.0864 (17) | −0.0017 (7) | −0.0114 (9) | −0.0125 (10) |
Cl1—C7 | 1.737 (2) | C3—C4 | 1.503 (3) |
Cl2—C9 | 1.734 (2) | C3—H3A | 0.91 (3) |
O1—C1 | 1.295 (3) | C3—H3B | 0.99 (3) |
O1—H1 | 0.92 (4) | C5—C10 | 1.380 (3) |
O2—C1 | 1.219 (3) | C5—C6 | 1.394 (3) |
O3—C4 | 1.225 (2) | C6—C7 | 1.378 (3) |
N1—C4 | 1.343 (3) | C6—H6 | 0.98 (3) |
N1—C5 | 1.415 (3) | C7—C8 | 1.372 (3) |
N1—H1A | 0.84 (3) | C8—C9 | 1.386 (3) |
C1—C2 | 1.488 (3) | C8—H8 | 0.93 (3) |
C2—C3 | 1.497 (4) | C9—C10 | 1.381 (3) |
C2—H2A | 0.90 (3) | C10—H10 | 0.92 (3) |
C2—H2B | 0.97 (3) | ||
C1—O1—H1 | 113 (2) | O3—C4—C3 | 121.8 (2) |
C4—N1—C5 | 125.67 (16) | N1—C4—C3 | 115.51 (17) |
C4—N1—H1A | 114.4 (19) | C10—C5—C6 | 120.6 (2) |
C5—N1—H1A | 119.8 (19) | C10—C5—N1 | 118.47 (19) |
O2—C1—O1 | 123.4 (2) | C6—C5—N1 | 121.0 (2) |
O2—C1—C2 | 123.1 (3) | C7—C6—C5 | 118.0 (2) |
O1—C1—C2 | 113.5 (2) | C7—C6—H6 | 124.9 (15) |
C1—C2—C3 | 113.79 (18) | C5—C6—H6 | 117.1 (15) |
C1—C2—H2A | 107.1 (18) | C8—C7—C6 | 123.18 (19) |
C3—C2—H2A | 111.1 (18) | C8—C7—Cl1 | 118.42 (18) |
C1—C2—H2B | 107.3 (16) | C6—C7—Cl1 | 118.39 (19) |
C3—C2—H2B | 114.0 (16) | C7—C8—C9 | 117.3 (2) |
H2A—C2—H2B | 103 (2) | C7—C8—H8 | 121.1 (17) |
C2—C3—C4 | 112.22 (18) | C9—C8—H8 | 121.6 (17) |
C2—C3—H3A | 111.7 (18) | C10—C9—C8 | 121.8 (2) |
C4—C3—H3A | 111.0 (17) | C10—C9—Cl2 | 119.54 (16) |
C2—C3—H3B | 110.6 (17) | C8—C9—Cl2 | 118.68 (19) |
C4—C3—H3B | 105.7 (17) | C5—C10—C9 | 119.2 (2) |
H3A—C3—H3B | 105 (2) | C5—C10—H10 | 118.7 (16) |
O3—C4—N1 | 122.7 (2) | C9—C10—H10 | 122.1 (16) |
O2—C1—C2—C3 | −7.0 (4) | C5—C6—C7—C8 | −0.6 (3) |
O1—C1—C2—C3 | 172.9 (2) | C5—C6—C7—Cl1 | 178.35 (15) |
C1—C2—C3—C4 | −174.8 (2) | C6—C7—C8—C9 | 0.9 (3) |
C5—N1—C4—O3 | 4.0 (4) | Cl1—C7—C8—C9 | −178.06 (14) |
C5—N1—C4—C3 | −176.1 (2) | C7—C8—C9—C10 | −0.4 (3) |
C2—C3—C4—O3 | −34.9 (4) | C7—C8—C9—Cl2 | 179.37 (15) |
C2—C3—C4—N1 | 145.1 (2) | C6—C5—C10—C9 | 0.6 (3) |
C4—N1—C5—C10 | 133.9 (2) | N1—C5—C10—C9 | 179.70 (17) |
C4—N1—C5—C6 | −47.0 (3) | C8—C9—C10—C5 | −0.3 (3) |
C10—C5—C6—C7 | −0.2 (3) | Cl2—C9—C10—C5 | 179.91 (15) |
N1—C5—C6—C7 | −179.26 (18) |
D—H···A | D—H | H···A | D···A | D—H···A |
N1—H1A···O3i | 0.84 (3) | 2.07 (3) | 2.904 (2) | 175 (2) |
O1—H1···O2ii | 0.92 (4) | 1.74 (4) | 2.658 (3) | 175 (4) |
C7—Cl1···Cgiii | 1.74 (1) | 3.54 (1) | 4.033 (2) | 93 (1) |
Symmetry codes: (i) x+1, y, z; (ii) −x+1, −y, −z; (iii) x−1, y, z. |
Experimental details
Crystal data | |
Chemical formula | C10H9Cl2NO3 |
Mr | 262.08 |
Crystal system, space group | Triclinic, P1 |
Temperature (K) | 296 |
a, b, c (Å) | 4.8568 (2), 8.6677 (4), 13.9038 (8) |
α, β, γ (°) | 74.467 (3), 80.495 (2), 82.712 (3) |
V (Å3) | 554.09 (5) |
Z | 2 |
Radiation type | Mo Kα |
µ (mm−1) | 0.58 |
Crystal size (mm) | 0.25 × 0.12 × 0.10 |
Data collection | |
Diffractometer | Bruker KappaAPEXII CCD diffractometer |
Absorption correction | Multi-scan (SADABS; Bruker, 2005) |
Tmin, Tmax | 0.870, 0.945 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 12157, 2971, 2065 |
Rint | 0.027 |
(sin θ/λ)max (Å−1) | 0.685 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.040, 0.125, 1.07 |
No. of reflections | 2971 |
No. of parameters | 172 |
H-atom treatment | Only H-atom coordinates refined |
Δρmax, Δρmin (e Å−3) | 0.27, −0.43 |
Computer programs: APEX2 (Bruker, 2007), SAINT (Bruker, 2007), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 1997) and PLATON (Spek, 2003), WinGX (Farrugia, 1999) and PLATON (Spek, 2003).
D—H···A | D—H | H···A | D···A | D—H···A |
N1—H1A···O3i | 0.84 (3) | 2.07 (3) | 2.904 (2) | 175 (2) |
O1—H1···O2ii | 0.92 (4) | 1.74 (4) | 2.658 (3) | 175 (4) |
C7—Cl1···Cgiii | 1.737 (2) | 3.5398 (11) | 4.033 (2) | 93.34 (7) |
Symmetry codes: (i) x+1, y, z; (ii) −x+1, −y, −z; (iii) x−1, y, z. |
Acknowledgements
The authors acknowledge the Higher Education Commision, Islamabad, Pakistan, for funding the purchase of the diffractometer. Dr Saqib Ali is also grateful to the PSF for financial support under project No. PSF/R&D/C–QU/Chem(270).
References
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Carboxylic acids catch the interest of people due to wide use of their metal complexes in biological and industrial field. On the other hand amino acids are one of the best sources to formulate the structure-activity correlation of metal derivatives as a biologically active agent (Nath et al., 2001) and widen the scope of investigation on the coordination behavior of the ligand in biological system. The title compound (I) has been prepared for complexation with different metals.
The structure of 3-(3-Nitrophenylaminocarbonyl)-propionic acid (Wardell et al., 2006) has been published. The title compound have replacement of 3-nitro with Cl and also an additional Cl-atom at 5-position of benzene ring. Therefore, the bond distances and packing of (I) is being compared with the mentioned reported structure. In (I) the C==O bond distances for carboxylate and carbonyl group have values of (C1==O2: 1.219 (3) Å) and (C4==O3: 1.225 (2) Å) in comparison to 1.223 (2) and 1.2214 (17) Å, respectively. The C—N bond distances are compareable within experimental errors. In both compounds similar intermolecular H-bonding (Table 1, Fig. 2) has been observed. The dihedral angle between the aromatic ring A(C5—C10) and (C1,C2,C3,O1,O2) have a value of 82.24 (8)°, whereas with (N1,C3,C4,O3) its value is 44.42 (12)°. The value of dihedral angle between (C1,C2,C3,O1,O2) and (N1,C3,C4,O3) is 38.36 (13)°. There exist a single C—Cl···π interaction at a distance of 3.5398 (11) Å [C7—CL1···CgAiii: symmetry code iii = -1 + x, y, z].