| Identification | Back Directory | [Name]
2-cyano-4-Methylpent-2-enoic acid | [CAS]
760-58-7 | [Synonyms]
2-cyano-4-Methylpent-2-enoic acid 2-Pentenoic acid, 2-cyano-4-methyl- | [Molecular Formula]
C7H9NO2 | [MOL File]
760-58-7.mol | [Molecular Weight]
139.15 |
| Chemical Properties | Back Directory | [Melting point ]
88 °C | [Boiling point ]
283.1±23.0 °C(Predicted) | [density ]
1.105±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [pka]
1.71±0.19(Predicted) | [Appearance]
White to off-white Solid | [InChI]
InChI=1S/C7H9NO2/c1-5(2)3-6(4-8)7(9)10/h3,5H,1-2H3,(H,9,10) | [InChIKey]
JYFREZOLRUHBAQ-UHFFFAOYSA-N | [SMILES]
C(O)(=O)C(C#N)=CC(C)C |
| Hazard Information | Back Directory | [Synthesis]
To a methanolic (200 mL) solution of cyanoacetic acid (8.7 g, 102 mmol) was added isobutyraldehyde (18.6 mL, 204 mmol) and the solution was stirred and a slight exothermic phenomenon was observed.After 30 min, piperidine (11.1 mL, 112 mmol) was added and stirring was continued for 1 hr. Subsequently, the solvent was removed by vacuum distillation under mild heating conditions. The crude product was diluted with ether and washed sequentially with 125 mL of 1.0 M HCl and brine. The organic phase was dried over anhydrous sodium sulfate and concentrated to give 11.2 g of a colorless oil, 2-cyano-4-methylpent-2-enoic acid, which precipitates on standing. | [References]
[1] Organic Process Research and Development, 2014, vol. 18, # 1, p. 109 - 121 [2] Patent: WO2012/25861, 2012, A1. Location in patent: Page/Page column 22 [3] Journal of the Chemical Society, 1932, p. 445,453 [4] Journal of the Chemical Society, 1933, p. 613 [5] Patent: WO2014/39899, 2014, A1. Location in patent: Page/Page column 52 |
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