Synthesis and Molecular Structures of (e)-non-2-enoic Acid and (e)-dec-2-enoic Acid

The molecular structures of (E)-non-2-enoic acid (C9) and (E)-dec-2-enoic acid (C10) are reported. The title compounds were crystallized by slow evaporation of ethanolic solutions at −30 °C. C9 crystallizes in the monoclinic space group P21/c and C10 in the triclinic space group P-1, each with 4 molecules in the unit cell. The unit cell parameters for


Introduction
Unsaturated fatty acids and particularly essential fatty acids are compounds with great interest in food, nutrition and health sciences due to their role in biological processes especially for humans [1][2][3][4].They can be classified as monounsaturated and polyunsaturated, or trans-unsaturated and cis-unsaturated fatty acids, which exhibit long nonpolar unsaturated alkyl chains and polar carboxylic head groups.For example, oleic acid (Z)-octadec-9-enoic acid, or linoleic acid (9Z,12Z)-9,12-octadecadienoic acid, respectively, can be found in natural foods, like meat, milk products, nuts, olives and oils.By increasing OPEN ACCESS the number of double bonds within the alkyl chain the melting point decreases, yielding liquids, especially in case of polyunsaturated fatty acids at ambient conditions [5].A certain number of derivatives of the title compounds (E)-non-2-enoic acid (C9) and (E)-dec-2-enoic acid (C10) exhibit interesting properties, e.g., 10-Hydroxy-2-decenoic acid isolated from royal jelly shows good antibiotic activity against many bacteria and fungi [6,7].4-hydroxy-trans-2-nonenoic acid as a derivate of C9 acts as a receptor ligand in the cerebral cortex and hippocampus and elevated concentrations can be found in patients with Alzheimer's and Parkinson's disease [8].

Synthesis
One-hundred and thirty years ago, Schneegans reported on the synthesis of nonenoic acid via reaction of heptanal, sodium acetate and acetic anhydride without knowledge of the correct constitution of this α,β-unsaturated carboxylic acid [25].Later, Harding and Weizmann reported on the correct molecular formula of the received (E)-non-2-enoic acid [26].However, until now there has been no X-ray determination of the crystal structure of C9 or its homologue C10.The syntheses of the two unsaturated α,β-carboxylic acids C9 and C10 are conducted by a convenient adapted condensation reaction of malonic acid and the appropriate aldehydes at room temperature in high yields and purities as depicted in Scheme 1 [27][28][29][30].Scheme 1. Reaction sequences for the synthesis of the two title compounds C9 and C10.

Crystal Structures
Molecular structures of linked acid dimers of the title compounds with pairs of O-H•••O hydrogen bonds are shown in Figures 1 and 2, respectively, with atom-labeling scheme and displacement thermal ellipsoids at the 50% probability level.Crystal and instrumental parameters of the crystal structure determinations of C9 and C10 can be found in Table 1.
Selected bond lengths and angles are summarized in Table 2. C9 crystallizes in monoclinic space group P21/c with 4 molecules in the unit cell, whereas C10 crystallizes in the triclinic space group P-1 with two symmetry independent molecules in the asymmetric unit and Z = 4.

General Considerations
NMR spectra were recorded on a Bruker AV300 or Bruker AV400 and chemical shifts of the 1 H, and 13 C spectra were reported in parts per million (ppm) using the solvent shifts for 1 H and 13 C as internal standard (CDCl3: 1 H δ = 7.26, 13 C δ = 77.0).Elemental analysis for C, and H was performed on a Leco Microanalysator TruSpec CHNS device.MS spectra were determined by electron spray ionization using a Thermo Electron Finnigan MAT 95-XP mass spectrometer.Melting points were determined by cyclic differential scanning calorimetry (DSC) using a Mettler Toledo DSC823 e in the range of −50 to 50 °C with a heating rate of 10 K/min (2 cycles, N2 atmosphere, Al crucible).All melting points are peak temperatures.

Materials
All chemicals were used as received without further drying or purification unless otherwise noted.n-heptanal, n-octanal, and malonic acid were purchased from ABCR (purity > 98%).

General Synthesis of α,β-unsaturated Carboxylic acids
Malonic acid (25.0 g, 240.2 mmol, 1.0 eq) was dissolved in dry pyridine (38.0 g, 480.5 mmol, 2.0 eq) at room temperature in a three-necked flask equipped with a magnetic stir bar and a reflux condenser under a mild flow of argon.The appropriate aldehyde (240.2 mmol, 1.0 eq) was then added in one portion and the resulting clear solution was further stirred for 72 h at room temperature under argon.Afterwards, the resulting light yellow to orange solution was brought to an acidic pH value by adding phosphoric acid at 0 °C (42.5 wt.%, 138.5 g, 600.6 mmol, 2.5 eq).The resulting two layers were extracted three times with 150 mL portions of ethyl acetate and reduced to a volume of ca. 150 mL in vacuo.To remove impurities from aldol condensation the raw acid was converted into the corresponding sodium salt by addition of an aqueous solution of sodium carbonate (20.4 g, 192.2 mmol, 0.8 eq in 200 mL).After stirring for 30 min the water phase was separated and extracted three times with 150 mL portions of ethyl acetate.The water phase was then acidified with concentrated hydrochloric acid (37.0 wt.%, 35.5 g, 360.4 mmol, 1.5 eq), the organic phase was separated and the water phase was again extracted three times with 150 mL portions of ethyl acetate.The combined organic phases were dried over Na2SO4 and evaporated to dryness in vacuo.The resulting raw product was further purified by distillation in vacuo yielding the product in purity > 99% (GC).

Crystal Structure Determinations
Data were collected on a Bruker Kappa APEX II Duo diffractometer [34].The structures were solved by direct methods and refined by full-matrix least-squares procedures on F 2 with the SHELXTL software package [35].Data were corrected for absorption effects using the multi-scan method (SADABS) [36].All non-hydrogen atoms were refined anisotropically.H1 could be found from the difference Fourier map and was refined with Uiso(H) fixed at 1.5 Ueq(O) for both compounds.For compound C10 the carboxyl group of the second molecule is disordered, therefore H3A and H4A were placed using AFIX 83 instruction with site occupancy factors of 0.6 for H3A and 0.4 for H4A (d(O-H) = 0.84 Å, Uiso(H) fixed at 1.5 Ueq(O)).The disorder concerning O3 and O4 was not resolved.All other H atoms were placed in idealized positions with d(C-H) = 0.95 Å (CH), 0.99 Å (CH2), 0.98 Å (CH3) and refined using a riding model with Uiso(H) fixed at 1.2 Ueq(C) for CH and CH2 and 1.5 Ueq(C) for CH3.Crystal data, data collection, and refinement parameters are collected in Table 1.DIAMOND program package was used for graphical representations [37].Crystallographic data for the structural analyses have been deposited with the Cambridge Crystallographic Data Centre, CCDC-1408770 for (E)-non-2-enoic acid (C9), and CCDC-1408769 for (E)-dec-2-enoic acid (C10).These data can be obtained free of charge via http://www.ccdc.cam.ac.uk or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB21EZ, UK; Fax: (+44)-1223-336-033; or E-Mail: deposit@ccdc.cam.ac.uk.

Conclusions
The crystal and molecular structures of two homologues in the series of α,β-unsaturated carboxylic acids, namely (E)-non-2-enoic acid (C9) and (E)-dec-2-enoic acid (C10), are reported.In analogy to other known crystal structures of this class of substances C9 and C10 are characterized by carboxylic acid inversion dimers linked by pairs of O-H•••O hydrogen bonds.However, in contrast to previously reported structures, C10 features two symmetry-independent molecules.

Figure 1 .
Figure 1.View of acid dimer molecules in the crystal of C9 showing atom labeling scheme.Displacement ellipsoids are drawn at the 50% probability level.

Figure 2 .
Figure 2. View of acid dimers of the two symmetry independent molecules in the crystal of C10 showing atom labeling scheme.Displacement ellipsoids are drawn at the 50% probability level.

Figure 3 .
Figure 3.View of the packing of acid dimer layers in the crystal of C9 along the crystallographic b axis.

Figure 4 .
Figure 4. View of the packing of acid dimer molecules in the crystal of C10 along the crystallographic a axis.

Table 1 .
Crystal data and structure refinement for compounds C9 and C10.