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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275502Generated: October 29, 2026

(Acetyloxy)acetonitrile → (Acetyloxy)acetonitrile

https://huagongshe.com/reaction/275502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Acetyloxy)acetonitrileHCID 13843—
ReactantSodiumHCID 5360545—
ReactantHCID 15767077HCID 15767077—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventDichloromethaneHCID 6344—
Product(Acetyloxy)acetonitrileHCID 13843—
ProductHCID 15767078HCID 15767078—

Reaction Steps

Cyanomethyl acetate was prepared according to the method described in Synth. Commun. 2, 215 (1972). A mixture of 2.78 g (10 millimole) of tetrabutylammonium chloride and 1 g (10 millimole) of cyanomethyl acetate was dissolved in 10 ml of dichloromethane. To the reaction mixture were added 2 g (9.6 millimoles) of N-formyl-2,6 dichloro-4-fluoroaniline and 3 ml (12 millimoles) of a 4 mole/l sodium hydroxyde aqueous solution. After stirring for 1 hour at room temperature, N-cyanomethyl-N-formyl-2,6-dichloro-4-fluoroaniline was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05393913
Source datasetuspto-grants-1995_02
ORD IDord-37806c01b6be454aa580efc0e855b3bd
Source noteuspto-grants-1995_02