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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721284Generated: November 2, 2026

Water → 2-Methylbenzoyl cyanide

https://huagongshe.com/reaction/1721284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
Reactant2-Methylbenzoyl chlorideHCID 70276—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product2-Methylbenzoyl cyanideHCID 9833990—

Reaction Steps

To a stirred solution of o-toluoyl chloride (38.86 g) in dichloromethane (250 ml) at room temperature was added water (20.0 ml) followed immediately by tetrabutylammonium bromide (0.15 g) and sodium cyanide (13.0 g). The reaction mixture was stirred vigorously for 11/2 hours, then filtered. The filtrate was washed with water (2×100 ml) then dried (MgSO4) and evaporated under reduced pressure to give a golden oil. Distillation under vacuum gave 2-methylbenzoyl cyanide, as a colourless oil, bp 47°-50°/0.05 mm. To 85% w/w sulphuric acid (140 ml) at room temperature was added sodium bromide (20 g) followed immediately by the dropwise addition of 2-methylbenzoyl cyanide (34.8 g). The reaction mixture was then heated gently until the exothermic reaction started and then maintained at 70° C. for 10 minutes by cooling. Methanol (400 ml) was added and the mixture heated under reflux for 1 hour, cooled and diluted with ice/water (500 ml). Extraction with diethyl ether gave a golden oil which was distilled under vacuum to give methyl oxo(o-tolyl)acetate, as B colourless oil, bp 75°-85°/0.4 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510344
Source datasetuspto-grants-1996_04
ORD IDord-43b7efd500324e4eaedd85229938f782
Source noteuspto-grants-1996_04