Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788976Generated: October 30, 2026

Acetic Anhydride → HCID 53655523, compound

https://huagongshe.com/reaction/1788976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-Oxo-3-(2,3,4,5-tetrafluorophenyl)propanenitrileHCID 13911786—
ReactantEthylorthoformateHCID 53630039—
ProductHCID 53655523HCID 5365552388%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-(2,3,4,5-tetrafluorobenzoyl)acetonitrile (13.1 g), ethyl orthoformate (13.4 g) and acetic anhydride (15.4 g) is heated at 100° C. with stirring for 3 hours. The reaction mixture is concentrated under vacuum to yield an orange brownish oily residue. When the oily residue is allowed to stand at room temperature, it crystallizes slowly. The resulting crystals are collected and washed successively with a 2:1 mixture of hexane and ethyl acetate, and a 5:1 mixture of hexane and ethyl acetate to give 3-ethoxy-2-(2,3,4,5-tetrafluorobenzoyl)acrylonitrile (14.5 g) as light orange crystals, m.p. 99°-101° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04686221
Source datasetuspto-grants-1987_08
ORD IDord-f4e9bacf1cdc4752baaef28e79f8c8f7
Source noteuspto-grants-1987_08