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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297231Generated: October 31, 2026

Acetic Acid → Methyl 2-cyano-4-methylpent-2-enoate

https://huagongshe.com/reaction/1297231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantIsobutyraldehydeHCID 6561—
ReactantMethyl cyanoacetateHCID 7747—
ReactantAmmonium AcetateHCID 517165—
SolventBenzeneHCID 241—
ProductMethyl 2-cyano-4-methylpent-2-enoateHCID 53793275—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of isobutyraldehyde (18.2 mL, 200 mmol) in dry benzene (20 mL) was added methyl cyanoacetate (18 mL, 200 mmol), ammonium acetate (2 g) and glacial acetic acid (4 mL). The reaction mixture was' stirred at 60° C. for 30 minutes and allowed to cool to room temperature. Excess of solvents was removed in vacuo and the residue was dissolved in EtOAc (200 mL). The organic layer was washed with water, dried over sodium sulfate and evaporated to give 2-cyano-4-methyl-pent-2-enoic acid methyl ester as pale yellow oil. Further purification of the pale yellow oil by distillation (7 mm Hg) gave product 2 (27.4 g, 56%) as colorless oil: 1H NMR (300 MHz, CDCl3) δ 1.16 (d, J=6.6 Hz, 6H), 2.96-3.04 (m, 1H), 3.87 (s, 3H), 7.47 (d, J=10.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250433B2
Source datasetuspto-grants-2007_07
ORD IDord-df4e111da33945948d792734eb28e3c6
Source noteuspto-grants-2007_07