ChemicalBook--->CAS DataBase List--->760-58-7

760-58-7

760-58-7 Structure

760-58-7 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H332-H335-H312-H315-H302
[Precautionary statements ]

P280-P302+P352-P312-P322-P363-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312
Hazard InformationBack Directory
[Synthesis]

Cyanoacetic acid

372-09-8

Isobutyraldehyde

78-84-2

2-cyano-4-Methylpent-2-enoic acid

760-58-7

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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