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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597685Generated: October 26, 2026

N,N-Dimethylaniline → 2-(4-Methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrile

https://huagongshe.com/reaction/597685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosgeneHCID 6371—
Reactant4-Methoxybenzyl alcoholHCID 7738—
Reactant2-(Hydroxyimino)-2-phenylacetonitrileHCID 69998—
Reactant2-Chlorocarbonyloxyimino-2-phenylacetonitrileHCID 53654775—
SolventBenzeneHCID 241—
SolventPyridineHCID 1049—
Product2-(4-Methoxybenzyloxycarbonyloxyimino)-2-phenylacetonitrileHCID 3916227—

Reaction Steps

A solution of dimethylaniline (6.0 ml.) in benzene (15 ml.) was added dropwise to a suspension of 2-hydroxyimino-2-phenylacetonitrile (7.3 g.) and phosgene (5.0 g.) in benzene (50 ml.) for 40 minutes under ice-cooling. The mixture was stirred for 2 hours at the same temperature and allowed to stand overnight. A solution of 4-methoxybenzyl alcohol (6.9 g.) and pyridine (4.0 ml.) in benzene (20 ml.) was added dropwise, for 30 minutes under ice-cooling to the mixture containing 2-chlorocarbonyloxyimino-2-phenylacetonitrile. The mixture was stirred for 7 hours at room temperature. The reaction mixture was then washed with water, 1N hydrochloric acid, water, a sodium bicarbonate aqueous solution and water, and dried over magnesium sulfate. The solution was concentrated and the residual crystals were triturated in n-hexane and collected by filtration. The crystals were recrystallized from a mixture of ethyl acetate and n-hexane to give 2-(4-methoxybenzyl)oxycarbonyloxyimino-2-phenylacetonitrile (3.1 g.). Mp 112° to 113° C. The mother liquor was concentrated to give the desired compound (2.4 g.). Total yield (5.5 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014915
Source datasetuspto-grants-1977_03
ORD IDord-5a276a56c8254b44ae828871b9d433ce
Source noteuspto-grants-1977_03