Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401827Generated: October 30, 2026

Water → 4-(4-Chlorophenyl)-3-oxobutanenitrile

https://huagongshe.com/reaction/401827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCyanoacetic acidHCID 9740—
Reactant(4-Chlorophenyl)acetic acidHCID 15880—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 178418918HCID 178418918—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Chlorophenyl)-3-oxobutanenitrileHCID 5098884782.1%

Reaction Steps

2 M of isopropylmagnesium chloride in THF (300 mL) was added to a −78° C. solution of cyanoacetic acid (28.3 g, 333 mmol) in anhydrous THF (600 mL, 7000 mmol). After 1 h, a solution of 4-chlorophenylacetic acid (20 g, 100 mmol) and N,N-carbonyldiimidazole (21.7 g, 134 mmol) in anhydrous THF (200 mL, 2000 mmol) was added. The reaction mixture was warmed to rt. After 16 h, the reaction mixture was poured into water (1 L, 60000 mmol). The mixture was adjusted to pH 4 with glacial AcOH. Gas evolution was evident during addition of the AcOH. The mixture was concentrated in vacuo to remove the THF (in 1 L portions). The product crystallized from the aqueous portions. The solid was collected by filtration, washing with water. Dried under vacuum to afford the product as a fluffy light orange-yellow solid (15.89 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741934B2
Source datasetuspto-grants-2014_06
ORD IDord-c02f0899bb2641fd8102ff6153ecff8a
Source noteuspto-grants-2014_06