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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263374Generated: November 1, 2026

4-(Trifluoromethyl)thiobenzamide → 4-(3-Benzyloxy-propyl)-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2263374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)thiobenzamideHCID 2734823—
Reactant6-Benzyloxy-2-chloro-3-oxo-hexanoic acid ethyl esterHCID 59295398—
SolventEthanolHCID 702—
Product4-(3-Benzyloxy-propyl)-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl esterHCID 5959476666.5%

Reaction Steps

To a solution of 1.15 g of 6-benzyloxy-2-chloro-3-oxo-hexanoic acid ethyl ester in 10 ml of ethanol was added 0.932 g of 4-(trifluoromethyl)thiobenzamide. The reaction mixture was refluxed overnight. The solvent was removed under reduced pressure. The resulting residue was taken into ethyl acetate, washed with water. The aqueous layer was separated and extracted with ethyl acetate. The combined organic extracts were washed with water, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel (heptane 90/ethyl acetate 10) to give 1.15 g of 4-(3-benzyloxy-propyl)-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851493B2
Source datasetuspto-grants-2010_12
ORD IDord-85d0d2fc56d643b3b8706997f63d33f0
Source noteuspto-grants-2010_12