Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490708Generated: October 28, 2026

4-(Trifluoromethyl)thiobenzamide → HCID 69055671, compound

https://huagongshe.com/reaction/490708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)thiobenzamideHCID 2734823—
ReactantMethyl 4-bromo-3-oxoheptanoateHCID 71356077—
SolventEthanolHCID 702—
ProductHCID 69055671HCID 6905567199.2%

Reaction Steps

4-Bromo-3-oxo-heptanoic acid methyl ester (6.0 g, 25.0 mmol) is dissolved into denatured ethanol (100 mL) and para-trifluoromethyl thiobenzamide (5.0 g, 24.4 mmol) is added in one portion. The reaction is purged of air and flushed with nitrogen then heated to reflux. The reaction is monitored by TLC and HPLC and when complete, the reaction is allowed to cool to room temperature. The solvent is removed and the reaction is diluted with ethyl acetate (200 mL), followed by washes with saturated sodium bicarbonate solution, water, and brine. The ethyl acetate solution is dried over anhydrous sodium sulfate, then concentrated and further purified using flash column chromatography (10% EtOAc/Hexanes) to yield pure [[5-Propyl-2-(4-trifluoromethyl-phenyl)-thiazol-4-yl]-acetic acid methyl ester (8.66 g, 24.2 mmol) or 98% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528160B2
Source datasetuspto-grants-2009_05
ORD IDord-1f4b3dd533d043e99d036a292f2e4b24
Source noteuspto-grants-2009_05