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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156593Generated: October 27, 2026

(Chlorothio)formyl chloride → Ethyl 2,3-dihydro-2-oxo-4-phenyl-5-thiazolecarboxylate

https://huagongshe.com/reaction/1156593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Chlorothio)formyl chlorideHCID 75990—
ReactantEthyl 3-amino-3-phenylprop-2-enoateHCID 312934—
SolventChlorobenzeneHCID 7964—
ProductEthyl 2,3-dihydro-2-oxo-4-phenyl-5-thiazolecarboxylateHCID 1304181555%

Reaction Conditions

Temperature110 °C

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-ebb93e671a914eccbdecaa4530183450
Source noteuspto-grants-1982_06