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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156594Generated: October 30, 2026

Phosphorus oxychloride → Ethyl 2-chloro-4-phenyl-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1156594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantEthyl 2,3-dihydro-2-oxo-4-phenyl-5-thiazolecarboxylateHCID 13041815—
ProductEthyl 2-chloro-4-phenyl-1,3-thiazole-5-carboxylateHCID 1304181668%

Reaction Steps

To a solution of 20.0 g (0.105 mole) of ethyl β-amino-cinnamate in 40 ml. of chlorobenzene under ice cooling was added a solution of 11.6 g (0.112 mole) of chorocarbonylsulfenyl chloride in 10 ml. of chlorobenzene. The reaction mixture was heated at 110° C. for 2 hours, cooled to triturated with petroleum ether. The precipitate was heated with hot benzene, cooled and filtered to give 14.4 g (55%) of ethyl 2,3-dihydro-2-oxo-4-phenyl-5-thiazolecarboxylate as yellow needles. A mixture of 3.0 g (0.012 mole) of ethyl 2,3-dihydro-2-oxo-4-phenyl-5-thiazolecarboxylate and 14 ml. of phosphorus oxychloride was held at reflux for 24 hours and cooled. The reaction mixture was poured into ice water. The solid precipitate was extracted into ether. The ether solution was dried and concentrated under reduced pressure. The residue was recrystallized from hexane to give 2.2 g (68%) of ethyl 2-chloro-4-phenyl-5-thiazolecarboxylate, m.p. 56°-57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336389
Source datasetuspto-grants-1982_06
ORD IDord-1d9caf51ec7f40219bc0aa16eebc46db
Source noteuspto-grants-1982_06