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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286274Generated: October 30, 2026

Acetic Anhydride → HCID 13060845, compound

https://huagongshe.com/reaction/2286274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactantp-Chlorophenacyl bromideHCID 68303—
ReactantBromo(phenyl)acetic acidHCID 97919—
ReactantAmmonium dithiocarbamateHCID 11083854—
ReactantHCID 178527837HCID 178527837—
SolventAcetic AcidHCID 176—
SolventAcetoneHCID 180—
ProductHCID 13060845HCID 1306084558%

Reaction Steps

A mixture of 10.0 g. (0.044 m.) 4-(4-chlorophenyl)-2-mercaptothiazole (prepared by the reaction of α-bromo-4-chloroacetophenone with ammonium dithiocarbamate) and 10.0 g. (0.04 m.) α-bromophenylacetic acid in 200 ml. of acetone and 40 ml. each of glacial acetic acid and acetic anhydride is heated for 2 hours. After the solvents are removed, the residual solid is triturated with acetone and the resulting solid collected. 10 g. (58% yield) of the title product is obtained, m.p. 160°-165° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04327221
Source datasetuspto-grants-1982_04
ORD IDord-5875f1818272432c94a097031811a804
Source noteuspto-grants-1982_04