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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087100Generated: October 27, 2026

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

https://huagongshe.com/reaction/1087100

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 11.22g of 2,2,2,-trifluorothioacetamide and 10.14g 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 100ml 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 3.74g of ethyl 2-(trifluoromethyl)-5-thiazolecarboxylate as yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034404
Source datasetuspto-grants-1991_07
ORD IDord-948b288d5fdb46548c04ba9b5338c401
Source noteuspto-grants-1991_07