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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781588Generated: October 26, 2026

Ethyl (chloroformyl)acetate → Ethyl 2-(trifluoromethyl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1781588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (chloroformyl)acetateHCID 118030—
ReactantTrifluoroethanethioamideHCID 4425751—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-(trifluoromethyl)-1,3-thiazole-5-carboxylateHCID 1517112624.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 11.22 g of 2,2,2,-trifluorothioacetamide and 10.14 g of ethyl 2-chloro-2-formylacetate was stirred for 30 minutes in an oil bath of 70° C. and then for 1.5 hours in an oil bath of 100° C., to which 100 ml of dichloromethane were added. After removing an insoluble substance, the mixture was concentrated and the residue was subjected to a column chromatography [developing solvent: hexane-ethyl acetate (10:1)], to obtain 3.74 g of ethyl 2-(trifluoromethyl)-5-thiazolecarboxylate as yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633375
Source datasetuspto-grants-1997_05
ORD IDord-e77115f6fff944f5b5d1ed887385f92e
Source noteuspto-grants-1997_05