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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746112Generated: October 29, 2026

Ethyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate → ethyl 2-Ethoxy-4-Trifluoromethyl-5-Thiazolecarboxylate

https://huagongshe.com/reaction/746112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylateHCID 1235240—
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
Productethyl 2-Ethoxy-4-Trifluoromethyl-5-ThiazolecarboxylateHCID 1328276378%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a cold (0° C.) solution of sodium ethoxide, prepared from 0.46 g (0.02 mole) of sodium and 40 ml. of dried ethanol, was added 5.2 g (0.02 mole) of ethyl 2-chloro-4-trifluoromethyl-5-thiazolecarboxylate. A precipitate formed immediately. The reaction mixture was heated to 80° C. and then poured into ice water. The precipitate was collected to give 4.2 g (78%) of the desired product as a white solid, m.p. 30.5°-31.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04602454
Source datasetuspto-grants-1986_07
ORD IDord-37de74abeaae4522a7dcc5fc580b9f92
Source noteuspto-grants-1986_07