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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597684Generated: October 30, 2026

N,N-Dimethylaniline → 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile

https://huagongshe.com/reaction/597684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantDiphosgeneHCID 10426—
Reactant2-(Hydroxyimino)-2-phenylacetonitrileHCID 69998—
Reactant2-Chlorocarbonyloxyimino-2-phenylacetonitrileHCID 53654775—
SolventAcetoneHCID 180—
SolventBenzeneHCID 241—
SolventPyridineHCID 1049—
Solventtert-ButanolHCID 6386—
Product2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—

Reaction Steps

A solution of 2-hydroxyimino-2-phenylacetonitrile (14.6 g.) and dimethylaniline (13.2 g.) in a mixture of acetone (5 ml.) and benzene (80 ml.) was added to a solution of trichloromethyl chloroformate (phosgene dimer) (6.7 ml.) in benzene (30 ml.) under ice-cooling. The mixture was stirred for 6 hours at the same temperature and allowed to stand overnight. A mixture of tert-butyl alcohol (11.1 g.), pyridine (16.0 ml.) and benzene (20 ml.) was added dropwise, under ice-cooling, to the resultant mixture containing 2-chlorocarbonyloxyimino- 2-phenyl-acetonitrile. The mixture was stirred for 7 hours at room temperature and allowed to stand overnight. The reaction mixture was treated as described in the above Examples 2(A) to 2(F) to give 2-tert-butoxycarbonyloxyimino-2-phenylacetonitrile (17.0 g.), mp 84° to 86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014915
Source datasetuspto-grants-1977_03
ORD IDord-80213ed12c7745878aa2c403264237ff
Source noteuspto-grants-1977_03