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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462136Generated: October 30, 2026

Acetic Anhydride → HCID 20453877, compound

https://huagongshe.com/reaction/1462136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 13122001HCID 13122001—
SolventWaterHCID 962—
ProductHCID 20453877HCID 20453877—

Reaction Steps

5-Amino-4-cyano-1-(2,3,6-trichloro-4-trifluoromethylphenyl)pyrazole (3.74 g) in acetic anhydride (20 ml) was heated at reflux for 6 hours. The reaction mixture was then evaporated under reduced pressure to remove unreacted acetic anhydride. The residual oil was dissolved in dichloromethane (50 ml) and filtered. The filtrate was evaporated to give a foam, which was then suspended in water (70 ml). The suspension was filtered and the filtrate deposited a solid on standing. The solid was collected by filtration and washed with water to give 5-acetamido-4-cyano-1-(2,3,6-trichloro-4-trifluoromethylphenyl)pyrazole (0.4 g), m.p. 177°-178° C., in the form of a fawn-coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04459150
Source datasetuspto-grants-1984_07
ORD IDord-0fbe4585ccd74e27bdad730164787c32
Source noteuspto-grants-1984_07