Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807045527/at2401sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807045527/at2401Isup2.hkl |
CCDC reference: 654273
To a solution containing 4-methoxy-N-(3,4-methylenedioxybenzylidene)-aniline (1.14 g, 5 mmol) and ethanol (20 ml), the borohydride sodium (0.76 g, 20 mmol) was added and stirred for 4 h (at 333–343 K), then acetone (10 ml) and water (20 ml) were added in turn, and the reaction mixture was cooled and the crude products were filtered off, washed with ethanol and dried. Colourless crystals of (I) suitable for X-ray structure analysis were obtained by recrystallizing the crude product from ethanol [m.p. 339–341 K].
H atoms were placed in calculated positions with C—H = 0.93 Å (aromatic), 0.97 Å (methylene) and 0.96 Å (methyl), N—H = 0.90 Å (amino), and refined in riding mode with Uiso(H) = 1.5Ueq(C) (methyl) and Uiso(H) = 1.2Ueq(C, N) (aromatic, methylene and amino). H atom on the amino group is disorder, which was identified from a difference Fourier map, the site occupancies were fixed at 0.5. The disordered H atoms were refined isotropically with riding mode.
The title compound, (I), was obtained by the reductive reaction of the schiff base, 4-methoxy-N-(3,4-methylenedioxybenzylidene)-aniline. we report here the crystal structure of (I).
The compounds (I) crystallizes in the orthorhombic space group Pbcn with Z = 8. As a result, the H1A and H1B bonded to N1 atom are disordered, each with 0.5 site occupancy (Fig. 1), the dihedral angles between the two benzene rings are 68.7 (2)°. Geometric parameters are normal (Allen et al., 1987) in (I).
In the crystal structure of (I), there are no classic hydrogen bonds. The molecules are connected by four weak C—H···π interactions with the distances in the range 3.55 (2) to 3.64 (2) Å, resulting in a three-dimensional structure (Table 1).
For related literature, see: Allen et al. (1987); Bernstein et al. (1995).
Data collection: SMART (Siemens, 1996); cell refinement: SAINT (Siemens, 1996); data reduction: SAINT (Siemens, 1996); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997a); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997a); molecular graphics: SHELXTL (Sheldrick, 1997b); software used to prepare material for publication: SHELXTL (Sheldrick, 1997b).
Fig. 1. A view of the title compund (I), showing the atom-numbering scheme. Displacement ellipsoids are drawn at the 30% probability level. | |
Fig. 2. Packing diagram. |
C15H15NO3 | Dx = 1.327 Mg m−3 |
Mr = 257.28 | Melting point: 339 K |
Orthorhombic, Pbcn | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: -P 2n 2ab | Cell parameters from 2390 reflections |
a = 54.050 (3) Å | θ = 2.8–21.7° |
b = 7.353 (1) Å | µ = 0.09 mm−1 |
c = 6.4830 (9) Å | T = 298 K |
V = 2576.5 (5) Å3 | Block, colourless |
Z = 8 | 0.52 × 0.49 × 0.45 mm |
F(000) = 1088 |
Bruker SMART CCD area-detector diffractometer | 2201 independent reflections |
Radiation source: fine-focus sealed tube | 1478 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.061 |
φ and ω scans | θmax = 25.0°, θmin = 1.5° |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | h = −64→41 |
Tmin = 0.953, Tmax = 0.959 | k = −8→8 |
9965 measured reflections | l = −6→7 |
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)] = 0.094 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.214 | H-atom parameters constrained |
S = 1.07 | w = 1/[σ2(Fo2) + (0.044P)2 + 7.8609P] where P = (Fo2 + 2Fc2)/3 |
2201 reflections | (Δ/σ)max < 0.001 |
173 parameters | Δρmax = 0.28 e Å−3 |
0 restraints | Δρmin = −0.29 e Å−3 |
C15H15NO3 | V = 2576.5 (5) Å3 |
Mr = 257.28 | Z = 8 |
Orthorhombic, Pbcn | Mo Kα radiation |
a = 54.050 (3) Å | µ = 0.09 mm−1 |
b = 7.353 (1) Å | T = 298 K |
c = 6.4830 (9) Å | 0.52 × 0.49 × 0.45 mm |
Bruker SMART CCD area-detector diffractometer | 2201 independent reflections |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | 1478 reflections with I > 2σ(I) |
Tmin = 0.953, Tmax = 0.959 | Rint = 0.061 |
9965 measured reflections |
R[F2 > 2σ(F2)] = 0.094 | 0 restraints |
wR(F2) = 0.214 | H-atom parameters constrained |
S = 1.07 | Δρmax = 0.28 e Å−3 |
2201 reflections | Δρmin = −0.29 e Å−3 |
173 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 | Occ. (<1) | |
N1 | 0.37308 (6) | 0.2577 (5) | 0.7958 (6) | 0.0443 (10) | |
H1A | 0.3836 | 0.2220 | 0.8954 | 0.053* | 0.50 |
H1B | 0.3765 | 0.3751 | 0.7687 | 0.053* | 0.50 |
O1 | 0.47087 (6) | 0.1691 (6) | 0.6437 (6) | 0.0680 (12) | |
O2 | 0.47446 (6) | 0.3279 (5) | 0.3376 (6) | 0.0621 (11) | |
O3 | 0.27794 (6) | 0.2373 (5) | 1.1237 (6) | 0.0570 (10) | |
C1 | 0.37902 (8) | 0.1547 (6) | 0.6126 (7) | 0.0457 (12) | |
H1C | 0.3668 | 0.1788 | 0.5067 | 0.055* | |
H1D | 0.3786 | 0.0257 | 0.6440 | 0.055* | |
C2 | 0.40408 (8) | 0.2046 (6) | 0.5346 (7) | 0.0366 (10) | |
C3 | 0.42537 (8) | 0.1544 (6) | 0.6460 (7) | 0.0436 (11) | |
H3 | 0.4242 | 0.0916 | 0.7701 | 0.052* | |
C4 | 0.44761 (8) | 0.2016 (6) | 0.5649 (7) | 0.0396 (11) | |
C5 | 0.45004 (8) | 0.2954 (6) | 0.3819 (7) | 0.0419 (11) | |
C6 | 0.42980 (9) | 0.3458 (7) | 0.2706 (8) | 0.0507 (13) | |
H6 | 0.4312 | 0.4090 | 0.1469 | 0.061* | |
C7 | 0.40707 (8) | 0.2980 (6) | 0.3510 (8) | 0.0456 (12) | |
H7 | 0.3930 | 0.3305 | 0.2776 | 0.055* | |
C8 | 0.48742 (10) | 0.2496 (9) | 0.5030 (10) | 0.0771 (19) | |
H8A | 0.4970 | 0.3425 | 0.5727 | 0.093* | |
H8B | 0.4988 | 0.1582 | 0.4512 | 0.093* | |
C9 | 0.34927 (7) | 0.2513 (6) | 0.8788 (7) | 0.0344 (10) | |
C10 | 0.34322 (8) | 0.3562 (6) | 1.0500 (7) | 0.0383 (11) | |
H10 | 0.3553 | 0.4287 | 1.1099 | 0.046* | |
C11 | 0.31982 (8) | 0.3557 (6) | 1.1336 (7) | 0.0421 (11) | |
H11 | 0.3163 | 0.4286 | 1.2472 | 0.051* | |
C12 | 0.30174 (8) | 0.2492 (6) | 1.0509 (7) | 0.0396 (11) | |
C13 | 0.30695 (8) | 0.1451 (6) | 0.8808 (7) | 0.0429 (11) | |
H13 | 0.2945 | 0.0744 | 0.8220 | 0.051* | |
C14 | 0.33044 (8) | 0.1440 (6) | 0.7956 (7) | 0.0402 (11) | |
H14 | 0.3337 | 0.0711 | 0.6816 | 0.048* | |
C15 | 0.27188 (10) | 0.3404 (9) | 1.3020 (9) | 0.0772 (19) | |
H15A | 0.2819 | 0.3011 | 1.4157 | 0.116* | |
H15B | 0.2547 | 0.3230 | 1.3352 | 0.116* | |
H15C | 0.2749 | 0.4670 | 1.2755 | 0.116* |
U11 | U22 | U33 | U12 | U13 | U23 | |
N1 | 0.034 (2) | 0.052 (2) | 0.047 (2) | −0.0017 (17) | −0.0002 (18) | −0.011 (2) |
O1 | 0.0409 (19) | 0.098 (3) | 0.065 (2) | −0.0062 (19) | −0.0082 (19) | 0.034 (2) |
O2 | 0.0409 (19) | 0.087 (3) | 0.058 (2) | −0.0027 (18) | 0.0128 (18) | 0.022 (2) |
O3 | 0.0356 (18) | 0.075 (2) | 0.060 (2) | −0.0044 (16) | 0.0113 (16) | −0.013 (2) |
C1 | 0.048 (3) | 0.046 (3) | 0.043 (3) | −0.003 (2) | −0.003 (2) | −0.007 (2) |
C2 | 0.038 (2) | 0.034 (2) | 0.038 (2) | −0.0043 (19) | 0.000 (2) | −0.003 (2) |
C3 | 0.048 (3) | 0.048 (3) | 0.034 (2) | 0.000 (2) | 0.004 (2) | 0.010 (2) |
C4 | 0.037 (2) | 0.044 (3) | 0.038 (3) | 0.002 (2) | 0.0003 (19) | 0.003 (2) |
C5 | 0.040 (3) | 0.043 (3) | 0.043 (3) | 0.000 (2) | 0.005 (2) | 0.006 (2) |
C6 | 0.053 (3) | 0.051 (3) | 0.048 (3) | 0.001 (2) | 0.002 (2) | 0.016 (3) |
C7 | 0.039 (2) | 0.047 (3) | 0.050 (3) | 0.007 (2) | −0.003 (2) | 0.003 (2) |
C8 | 0.042 (3) | 0.107 (5) | 0.082 (4) | −0.008 (3) | 0.005 (3) | 0.037 (4) |
C9 | 0.034 (2) | 0.034 (2) | 0.035 (2) | 0.0020 (18) | −0.002 (2) | 0.002 (2) |
C10 | 0.042 (3) | 0.036 (2) | 0.037 (2) | −0.002 (2) | −0.008 (2) | −0.005 (2) |
C11 | 0.042 (3) | 0.047 (3) | 0.037 (2) | 0.006 (2) | −0.004 (2) | −0.006 (2) |
C12 | 0.034 (2) | 0.041 (3) | 0.043 (3) | 0.002 (2) | −0.001 (2) | −0.003 (2) |
C13 | 0.034 (2) | 0.048 (3) | 0.046 (3) | −0.005 (2) | −0.002 (2) | −0.009 (2) |
C14 | 0.039 (2) | 0.044 (3) | 0.037 (3) | 0.000 (2) | 0.003 (2) | −0.015 (2) |
C15 | 0.056 (3) | 0.098 (5) | 0.077 (4) | −0.002 (3) | 0.026 (3) | −0.030 (4) |
N1—C9 | 1.396 (5) | C6—H6 | 0.9300 |
N1—C1 | 1.445 (6) | C7—H7 | 0.9300 |
N1—H1A | 0.9000 | C8—O2i | 3.074 (7) |
N1—H1B | 0.9000 | C8—O1ii | 3.267 (7) |
O1—C4 | 1.378 (5) | C8—H8A | 0.9700 |
O1—C8 | 1.408 (6) | C8—H8B | 0.9700 |
O2—C5 | 1.371 (5) | C9—C10 | 1.391 (6) |
O2—C8 | 1.405 (6) | C9—C14 | 1.396 (6) |
O3—C12 | 1.373 (5) | C10—C11 | 1.376 (6) |
O3—C15 | 1.420 (6) | C10—H10 | 0.9300 |
C1—C2 | 1.491 (6) | C11—C12 | 1.362 (6) |
C1—H1C | 0.9700 | C11—H11 | 0.9300 |
C1—H1D | 0.9700 | C12—C13 | 1.371 (6) |
C2—C7 | 1.384 (6) | C13—C14 | 1.385 (6) |
C2—C3 | 1.408 (6) | C13—H13 | 0.9300 |
C3—C4 | 1.357 (6) | C14—H14 | 0.9300 |
C3—H3 | 0.9300 | C15—H15A | 0.9600 |
C4—C5 | 1.379 (6) | C15—H15B | 0.9600 |
C5—C6 | 1.362 (6) | C15—H15C | 0.9600 |
C6—C7 | 1.380 (6) | ||
C9—N1—C1 | 120.3 (4) | O2—C8—O1ii | 162.5 (4) |
C9—N1—H1A | 107.3 | O1—C8—O1ii | 84.7 (3) |
C1—N1—H1A | 107.3 | O2i—C8—O1ii | 94.30 (17) |
C9—N1—H1B | 107.3 | O2—C8—H8A | 109.6 |
C1—N1—H1B | 107.3 | O1—C8—H8A | 109.6 |
H1A—N1—H1B | 106.9 | O2i—C8—H8A | 81.0 |
C4—O1—C8 | 105.5 (4) | O1ii—C8—H8A | 55.3 |
C5—O2—C8 | 104.4 (4) | O2—C8—H8B | 109.6 |
C12—O3—C15 | 117.5 (4) | O1—C8—H8B | 109.6 |
N1—C1—C2 | 110.6 (4) | O2i—C8—H8B | 57.1 |
N1—C1—H1C | 109.5 | O1ii—C8—H8B | 71.4 |
C2—C1—H1C | 109.5 | H8A—C8—H8B | 108.1 |
N1—C1—H1D | 109.5 | C10—C9—N1 | 120.4 (4) |
C2—C1—H1D | 109.5 | C10—C9—C14 | 116.8 (4) |
H1C—C1—H1D | 108.1 | N1—C9—C14 | 122.8 (4) |
C7—C2—C3 | 118.4 (4) | C11—C10—C9 | 122.0 (4) |
C7—C2—C1 | 121.3 (4) | C11—C10—H10 | 119.0 |
C3—C2—C1 | 120.2 (4) | C9—C10—H10 | 119.0 |
C4—C3—C2 | 117.3 (4) | C12—C11—C10 | 120.4 (4) |
C4—C3—H3 | 121.4 | C12—C11—H11 | 119.8 |
C2—C3—H3 | 121.4 | C10—C11—H11 | 119.8 |
C3—C4—O1 | 128.4 (4) | C11—C12—C13 | 119.4 (4) |
C3—C4—C5 | 123.1 (4) | C11—C12—O3 | 125.0 (4) |
O1—C4—C5 | 108.6 (4) | C13—C12—O3 | 115.7 (4) |
C6—C5—O2 | 127.9 (4) | C12—C13—C14 | 120.8 (4) |
C6—C5—C4 | 121.0 (4) | C12—C13—H13 | 119.6 |
O2—C5—C4 | 111.1 (4) | C14—C13—H13 | 119.6 |
C5—C6—C7 | 116.5 (4) | C13—C14—C9 | 120.7 (4) |
C5—C6—H6 | 121.8 | C13—C14—H14 | 119.6 |
C7—C6—H6 | 121.8 | C9—C14—H14 | 119.6 |
C6—C7—C2 | 123.7 (4) | O3—C15—H15A | 109.5 |
C6—C7—H7 | 118.1 | O3—C15—H15B | 109.5 |
C2—C7—H7 | 118.1 | H15A—C15—H15B | 109.5 |
O2—C8—O1 | 110.5 (4) | O3—C15—H15C | 109.5 |
O2—C8—O2i | 73.1 (3) | H15A—C15—H15C | 109.5 |
O1—C8—O2i | 165.9 (5) | H15B—C15—H15C | 109.5 |
C9—N1—C1—C2 | 171.2 (4) | C5—O2—C8—O1 | 0.7 (7) |
N1—C1—C2—C7 | −111.3 (5) | C5—O2—C8—O2i | 166.3 (3) |
N1—C1—C2—C3 | 69.7 (5) | C5—O2—C8—O1ii | −148.4 (13) |
C7—C2—C3—C4 | 0.0 (6) | C4—O1—C8—O2 | −1.0 (7) |
C1—C2—C3—C4 | 179.0 (4) | C4—O1—C8—O2i | −103.3 (15) |
C2—C3—C4—O1 | 179.8 (5) | C4—O1—C8—O1ii | 170.0 (3) |
C2—C3—C4—C5 | 0.3 (7) | C1—N1—C9—C10 | −177.3 (4) |
C8—O1—C4—C3 | −178.6 (5) | C1—N1—C9—C14 | 1.8 (7) |
C8—O1—C4—C5 | 0.9 (6) | N1—C9—C10—C11 | 178.8 (4) |
C8—O2—C5—C6 | 179.2 (5) | C14—C9—C10—C11 | −0.4 (7) |
C8—O2—C5—C4 | −0.1 (6) | C9—C10—C11—C12 | 0.8 (7) |
C3—C4—C5—C6 | −0.4 (7) | C10—C11—C12—C13 | −1.3 (7) |
O1—C4—C5—C6 | −179.9 (5) | C10—C11—C12—O3 | 179.2 (4) |
C3—C4—C5—O2 | 179.0 (4) | C15—O3—C12—C11 | −1.7 (7) |
O1—C4—C5—O2 | −0.5 (5) | C15—O3—C12—C13 | 178.9 (5) |
O2—C5—C6—C7 | −179.2 (5) | C11—C12—C13—C14 | 1.5 (7) |
C4—C5—C6—C7 | 0.1 (7) | O3—C12—C13—C14 | −179.0 (4) |
C5—C6—C7—C2 | 0.2 (7) | C12—C13—C14—C9 | −1.1 (7) |
C3—C2—C7—C6 | −0.2 (7) | C10—C9—C14—C13 | 0.5 (7) |
C1—C2—C7—C6 | −179.3 (4) | N1—C9—C14—C13 | −178.6 (4) |
Symmetry codes: (i) −x+1, y, −z+1/2; (ii) −x+1, y, −z+3/2. |
D—H···A | D—H | H···A | D···A | D—H···A |
C15—H15B···O3iii | 0.96 | 2.61 | 3.454 (6) | 147 |
C3—H3···Cg1iv | 0.93 | 2.82 | 3.64 (2) | 148 |
C6—H6···Cg1v | 0.93 | 2.75 | 3.55 (2) | 145 |
C11—H11···Cg2vi | 0.93 | 2.80 | 3.63 (2) | 150 |
C14—H14···Cg2vii | 0.93 | 2.76 | 3.59 (2) | 149 |
Symmetry codes: (iii) −x+1/2, −y+1/2, z+1/2; (iv) x, −y, z+1/2; (v) x, −y+1, z−1/2; (vi) x, −y+1, z+1/2; (vii) x, −y, z−1/2. |
Experimental details
Crystal data | |
Chemical formula | C15H15NO3 |
Mr | 257.28 |
Crystal system, space group | Orthorhombic, Pbcn |
Temperature (K) | 298 |
a, b, c (Å) | 54.050 (3), 7.353 (1), 6.4830 (9) |
V (Å3) | 2576.5 (5) |
Z | 8 |
Radiation type | Mo Kα |
µ (mm−1) | 0.09 |
Crystal size (mm) | 0.52 × 0.49 × 0.45 |
Data collection | |
Diffractometer | Bruker SMART CCD area-detector |
Absorption correction | Multi-scan (SADABS; Sheldrick, 1996) |
Tmin, Tmax | 0.953, 0.959 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 9965, 2201, 1478 |
Rint | 0.061 |
(sin θ/λ)max (Å−1) | 0.595 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.094, 0.214, 1.07 |
No. of reflections | 2201 |
No. of parameters | 173 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.28, −0.29 |
Computer programs: SMART (Siemens, 1996), SAINT (Siemens, 1996), SHELXS97 (Sheldrick, 1997a), SHELXL97 (Sheldrick, 1997a), SHELXTL (Sheldrick, 1997b).
D—H···A | D—H | H···A | D···A | D—H···A |
C3—H3···Cg1i | 0.93 | 2.82 | 3.64 (2) | 148.2 |
C6—H6···Cg1ii | 0.93 | 2.75 | 3.55 (2) | 144.8 |
C11—H11···Cg2iii | 0.93 | 2.80 | 3.63 (2) | 149.5 |
C14—H14···Cg2iv | 0.93 | 2.76 | 3.59 (2) | 149.0 |
Symmetry codes: (i) x, −y, z+1/2; (ii) x, −y+1, z−1/2; (iii) x, −y+1, z+1/2; (iv) x, −y, z−1/2. |
The title compound, (I), was obtained by the reductive reaction of the schiff base, 4-methoxy-N-(3,4-methylenedioxybenzylidene)-aniline. we report here the crystal structure of (I).
The compounds (I) crystallizes in the orthorhombic space group Pbcn with Z = 8. As a result, the H1A and H1B bonded to N1 atom are disordered, each with 0.5 site occupancy (Fig. 1), the dihedral angles between the two benzene rings are 68.7 (2)°. Geometric parameters are normal (Allen et al., 1987) in (I).
In the crystal structure of (I), there are no classic hydrogen bonds. The molecules are connected by four weak C—H···π interactions with the distances in the range 3.55 (2) to 3.64 (2) Å, resulting in a three-dimensional structure (Table 1).