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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389948Generated: October 31, 2026

Chloroacetyl chloride → HCID 54084673, compound

https://huagongshe.com/reaction/1389948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantHCID 20295995HCID 20295995—
SolventTolueneHCID 1140—
ProductHCID 54084673HCID 54084673—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3 parts of ethyl α-[(4-bromophenyl)amino]-2,3,6-trichlorobenzeneacetate and 4.5 parts of 2-chloroacetyl chloride is stirred for 4 hours at 80° C. The mixture is taken up twice in methylbenzene and the latter is evaporated each time. The oily residue solidifies on triturating in petroleumether. The latter is decanted and the residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding a first fraction of 1.7 parts of ethyl α-[(4-bromophenyl) (2-chloroacetyl)-amino]-2,3,6-trichlorobenzeneacetate; mp. 140.8° C. The mother liquor is concentrated and a second fraction of 1.2 parts of ethyl α-[(4-bromophenyl) (2-chloroacetyl)amino]-2,3,6-trichlorobenzeneacetate is filtered off.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04246429
Source datasetuspto-grants-1981_01
ORD IDord-4b3e795b4c624053b3e458cf977605b4
Source noteuspto-grants-1981_01