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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Trifluoromethyl)thiobenzamide | HCID 2734823 | — |
| Reactant | 6-Benzyloxy-2-chloro-3-oxo-hexanoic acid ethyl ester | HCID 59295398 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(3-Benzyloxy-propyl)-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester | HCID 59594766 | 66.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851493B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-85d0d2fc56d643b3b8706997f63d33f0 |
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| Source note | uspto-grants-2010_12 |
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