HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389948Generated: October 31, 2026
Chloroacetyl chloride → HCID 54084673, compound
https://huagongshe.com/reaction/1389948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | HCID 20295995 | HCID 20295995 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54084673 | HCID 54084673 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04246429 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-4b3e795b4c624053b3e458cf977605b4 |
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| Source note | uspto-grants-1981_01 |
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