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Acta Crystallogr Sect E Struct Rep Online. Jul 1, 2011; 67(Pt 7): o1585.
Published online Jun 4, 2011. doi:  10.1107/S1600536811021180
PMCID: PMC3151843
Ethyl 5-methyl-1H-pyrrole-2-carboxyl­ate
Zhao-Po Zhang,a Yuan Wang,a* and Xiao-Xia Lib
aDepartment of Physics and Chemistry, Henan Polytechnic University, Jiaozuo 454000, People’s Republic of China
bInstitute of Functional Materials, Jiangxi University of Finance and Economics, Nanchang 330013, People’s Republic of China
Correspondence e-mail: wangyuan08/at/hpu.edu.cn
Received June 1, 2011; Accepted June 1, 2011.
Abstract
In the title mol­ecule, C8H11NO2, the r.m.s. deviation of non-H atoms from their best plane is 0.031 Å. Mol­ecules are connected via a pair of N—H(...)O hydrogen bonds into a centrosymmetric dimer.
Related literature
For the crystal structure of the 5-cyano analogue of the title compound, see: Zhang et al. (2003 [triangle]). For the synthesis of the title compound, see: Motekaitis et al. (1970 [triangle]).
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Object name is e-67-o1585-scheme1.jpg Object name is e-67-o1585-scheme1.jpg
Crystal data
  • C8H11NO2
  • M r = 153.18
  • Monoclinic, An external file that holds a picture, illustration, etc.
Object name is e-67-o1585-efi1.jpg
  • a = 7.0759 (3) Å
  • b = 18.0705 (9) Å
  • c = 6.6606 (3) Å
  • β = 101.349 (3)°
  • V = 835.01 (7) Å3
  • Z = 4
  • Mo Kα radiation
  • μ = 0.09 mm−1
  • T = 296 K
  • 0.20 × 0.15 × 0.13 mm
Data collection
  • Bruker APEXII CCD diffractometer
  • Absorption correction: multi-scan (SADABS; Bruker, 2007 [triangle]) T min = 0.984, T max = 0.989
  • 7496 measured reflections
  • 1991 independent reflections
  • 1157 reflections with I > 2σ(I)
  • R int = 0.029
Refinement
  • R[F 2 > 2σ(F 2)] = 0.045
  • wR(F 2) = 0.143
  • S = 1.02
  • 1991 reflections
  • 102 parameters
  • H-atom parameters constrained
  • Δρmax = 0.16 e Å−3
  • Δρmin = −0.16 e Å−3
Data collection: APEX2 (Bruker, 2007 [triangle]); cell refinement: SAINT (Bruker, 2007 [triangle]); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 [triangle]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 [triangle]); molecular graphics: SHELXTL (Sheldrick, 2008 [triangle]); software used to prepare material for publication: SHELXTL.
Table 1
Table 1
Hydrogen-bond geometry (Å, °)
Supplementary Material
Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S1600536811021180/gk2381sup1.cif
Structure factors: contains datablock(s) I. DOI: 10.1107/S1600536811021180/gk2381Isup2.hkl
Supplementary material file. DOI: 10.1107/S1600536811021180/gk2381Isup3.cml
Additional supplementary materials: crystallographic information; 3D view; checkCIF report
Acknowledgments
The authors are grateful to the National Natural Science Foundation of China for financial support (grant No. 21001040).
supplementary crystallographic information
Comment
As part of our studies on hydrazone ligands bearing pyrrole unit the title compound was synthesized and characterized by X-ray diffraction.
The non-hydrogen atoms of the title molecule (Fig. 1) are situated in a fair plane (r.m.s. deviation of the non-hydrogen atoms being 0.0306 Å). In the crystal, the molecules are linked into a centrosymmetric dimer by two intermolecular N—H···O hydrogen bonds, forming a R22(10) ring motif (Table 1, Fig. 2).
Experimental
The title compound was synthesized according to the literature procedure (Motekaitis et al., 1970). The crude orange solid was washed well with ice water and dried in air. Colorless plates of the title compound were obtained by slow evaporation of petroleum ether/ethyl acetate (100:1) solution.
Refinement
All H atoms were placed in calculated positions, with C—H = 0.93–0.97 Å and N—H = 0.86 Å, and were thereafter treated as riding, with Uiso(H) values of 1.5Ueq(C) for methyl groups and 1.2Ueq(C,N) for others.
Figures
Fig. 1.
Fig. 1.
The title compound with the displacement ellipsoids shown at the 50% probability level.
Fig. 2.
Fig. 2.
The centrosymmetric dimer via N-H···O hydrogen bonds of the title compound (hydrogen bonds shown as dashed lines, symmetry code:: 1 - x, 1 - y, 2 - z).
Crystal data
C8H11NO2F(000) = 328
Mr = 153.18Dx = 1.218 Mg m3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybcCell parameters from 2070 reflections
a = 7.0759 (3) Åθ = 2.3–24.2°
b = 18.0705 (9) ŵ = 0.09 mm1
c = 6.6606 (3) ÅT = 296 K
β = 101.349 (3)°Plate, colorless
V = 835.01 (7) Å30.20 × 0.15 × 0.13 mm
Z = 4
Data collection
Bruker APEXII CCD diffractometer1991 independent reflections
Radiation source: fine-focus sealed tube1157 reflections with I > 2σ(I)
graphiteRint = 0.029
[var phi] and ω scansθmax = 27.9°, θmin = 2.3°
Absorption correction: multi-scan (SADABS; Bruker, 2007)h = −9→9
Tmin = 0.984, Tmax = 0.989k = −23→23
7496 measured reflectionsl = −8→8
Refinement
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.045Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.143H-atom parameters constrained
S = 1.02w = 1/[σ2(Fo2) + (0.0683P)2 + 0.0738P] where P = (Fo2 + 2Fc2)/3
1991 reflections(Δ/σ)max < 0.001
102 parametersΔρmax = 0.16 e Å3
0 restraintsΔρmin = −0.16 e Å3
Special details
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)
xyzUiso*/Ueq
O20.12507 (16)0.64959 (6)0.92921 (18)0.0629 (4)
N10.52408 (19)0.57393 (7)0.7402 (2)0.0581 (4)
H10.56370.53600.81460.087*
C60.2631 (2)0.60036 (9)0.9187 (3)0.0585 (4)
O10.2888 (2)0.54602 (8)1.0272 (2)0.0861 (5)
C50.3729 (2)0.61798 (9)0.7644 (2)0.0548 (4)
C20.6023 (2)0.59835 (10)0.5831 (3)0.0600 (5)
C8−0.1423 (3)0.69326 (11)1.0591 (3)0.0768 (6)
H8A−0.07940.74001.09160.115*
H8B−0.22680.68371.15270.115*
H8C−0.21590.69460.92170.115*
C40.3561 (2)0.67196 (10)0.6178 (3)0.0651 (5)
H40.26580.71000.59760.078*
C70.0051 (3)0.63353 (10)1.0768 (3)0.0691 (5)
H7A0.08250.63241.21420.083*
H7B−0.05690.58581.04800.083*
C10.7719 (3)0.56133 (11)0.5261 (3)0.0780 (6)
H1A0.88620.58930.57910.117*
H1B0.75430.55850.37960.117*
H1C0.78470.51230.58270.117*
C30.4987 (3)0.65956 (10)0.5044 (3)0.0712 (5)
H30.52000.68790.39440.085*
Atomic displacement parameters (Å2)
U11U22U33U12U13U23
O20.0581 (7)0.0624 (7)0.0748 (8)0.0073 (5)0.0294 (6)0.0035 (6)
N10.0533 (8)0.0560 (8)0.0691 (9)0.0001 (6)0.0221 (7)0.0000 (6)
C60.0519 (9)0.0563 (9)0.0698 (11)0.0019 (8)0.0182 (8)−0.0026 (9)
O10.0847 (10)0.0820 (9)0.1032 (11)0.0273 (8)0.0467 (8)0.0332 (8)
C50.0486 (9)0.0532 (9)0.0649 (11)−0.0015 (7)0.0165 (8)−0.0035 (8)
C20.0539 (9)0.0652 (10)0.0644 (11)−0.0091 (8)0.0202 (8)−0.0063 (8)
C80.0689 (12)0.0819 (13)0.0884 (15)0.0074 (10)0.0373 (11)−0.0054 (10)
C40.0587 (10)0.0616 (10)0.0766 (12)0.0036 (8)0.0172 (9)0.0060 (9)
C70.0635 (11)0.0788 (12)0.0716 (12)0.0050 (9)0.0293 (9)0.0048 (9)
C10.0664 (12)0.0894 (14)0.0867 (14)−0.0022 (10)0.0360 (10)−0.0094 (11)
C30.0683 (11)0.0781 (12)0.0715 (12)−0.0023 (10)0.0246 (10)0.0107 (10)
Geometric parameters (Å, °)
C2—C11.487 (2)C1—H1A0.9600
C2—C31.373 (3)C1—H1B0.9600
C4—C31.392 (2)C1—H1C0.9600
C5—C41.369 (2)C3—H30.9300
N1—C21.351 (2)C4—H40.9300
N1—C51.368 (2)C7—H7A0.9700
C6—C51.440 (2)C7—H7B0.9700
C6—O11.212 (2)C8—H8A0.9600
O2—C61.3333 (19)C8—H8B0.9600
O2—C71.4490 (19)C8—H8C0.9600
C8—C71.490 (2)N1—H10.8600
C6—O2—C7115.81 (13)C5—C4—C3107.57 (16)
C2—N1—C5110.53 (14)C5—C4—H4126.2
C2—N1—H1124.7C3—C4—H4126.2
C5—N1—H1124.7O2—C7—C8107.22 (15)
O1—C6—O2122.31 (15)O2—C7—H7A110.3
O1—C6—C5124.50 (15)C8—C7—H7A110.3
O2—C6—C5113.19 (15)O2—C7—H7B110.3
C4—C5—N1106.89 (14)C8—C7—H7B110.3
C4—C5—C6133.09 (16)H7A—C7—H7B108.5
N1—C5—C6119.97 (15)C2—C1—H1A109.5
N1—C2—C3106.81 (15)C2—C1—H1B109.5
N1—C2—C1121.69 (16)H1A—C1—H1B109.5
C3—C2—C1131.48 (17)C2—C1—H1C109.5
C7—C8—H8A109.5H1A—C1—H1C109.5
C7—C8—H8B109.5H1B—C1—H1C109.5
H8A—C8—H8B109.5C2—C3—C4108.20 (16)
C7—C8—H8C109.5C2—C3—H3125.9
H8A—C8—H8C109.5C4—C3—H3125.9
H8B—C8—H8C109.5
C7—O2—C6—O1−0.9 (2)C5—N1—C2—C3−0.1 (2)
C7—O2—C6—C5177.93 (14)C5—N1—C2—C1178.73 (15)
C2—N1—C5—C4−0.12 (19)N1—C5—C4—C30.26 (19)
C2—N1—C5—C6177.58 (14)C6—C5—C4—C3−177.02 (18)
O1—C6—C5—C4173.57 (18)C6—O2—C7—C8−178.10 (14)
O2—C6—C5—C4−5.3 (3)N1—C2—C3—C40.2 (2)
O1—C6—C5—N1−3.4 (3)C1—C2—C3—C4−178.40 (18)
O2—C6—C5—N1177.75 (13)C5—C4—C3—C2−0.3 (2)
Hydrogen-bond geometry (Å, °)
D—H···AD—HH···AD···AD—H···A
N1—H1···O1i0.861.992.8363 (19)167.
Symmetry codes: (i) −x+1, −y+1, −z+2.
Footnotes
Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: GK2381).
References
  • Bruker (2007). APEX2, SAINT and SADABS Bruker AXS Inc., Madison, Wisconsin, USA.
  • Motekaitis, R. J., Heinert, H. D. & Martell, A. E. (1970). J. Org. Chem. 35, 2504–2511.
  • Sheldrick, G. M. (2008). Acta Cryst. A64, 112–122. [PubMed]
  • Zhang, Y.-H., Yin, Z., Li, X.-F., He, J. & Cheng, J.-P. (2003). Acta Cryst. E59, o1881–o1882.
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