HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490708Generated: October 28, 2026
4-(Trifluoromethyl)thiobenzamide → HCID 69055671, compound
https://huagongshe.com/reaction/490708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Trifluoromethyl)thiobenzamide | HCID 2734823 | — |
| Reactant | Methyl 4-bromo-3-oxoheptanoate | HCID 71356077 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69055671 | HCID 69055671 | 99.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528160B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-1f4b3dd533d043e99d036a292f2e4b24 |
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| Source note | uspto-grants-2009_05 |
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