HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398481Generated: October 29, 2026
Methanol → 3-Cyclopentyl-2-(4-trifluoromethylsulfanylphenyl)propionic acid methyl ester
https://huagongshe.com/reaction/398481
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 22315105 | HCID 22315105 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | 3-Cyclopentyl-2-(4-trifluoromethylsulfanylphenyl)propionic acid methyl ester | HCID 46221383 | 99% |
Reaction Steps
A solution of 3-cyclopentyl-2-(4-trifluoromethylsulfanyl-phenyl)propionic acid (1.33 g, 4.18 mmol) in methanol (10 mL) was treated slowly with 4 drops of concentrated sulfuric acid. The resulting reaction mixture was heated under reflux for 36 h. The reaction mixture was allowed to cool to 25° C. and then concentrated in vacuo to remove methanol. The residue was diluted with ethyl acetate (200 mL). The organic phase was washed with a saturated aqueous sodium bicarbonate solution (1×100 mL) and a saturated aqueous sodium chloride solution (1×100 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 97/3 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(4-trifluoromethylsulfanyl-phenyl)propionic acid methyl ester (1.37 g, 99%) as a light yellow oil: EI-HRMS m/e calcd for C16H19F3O2S (M+) 332.1058, found 332.1052.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610846B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-b5ffa660849f444ea629729e543d9a2b |
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| Source note | uspto-grants-2003_08 |
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