HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767882Generated: October 25, 2026
[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-acetic acid → 2-[4-Methyl-2-[4-(trifluoromethyl)phenyl]-5-thiazolyl]ethanol
https://huagongshe.com/reaction/1767882
Participants
| Role | Name | HCID | Charge |
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| Reactant | [4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-acetic acid | HCID 17972178 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[4-Methyl-2-[4-(trifluoromethyl)phenyl]-5-thiazolyl]ethanol | HCID 22647583 | 100% |
Reaction Steps
A solution of [4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-acetic acid (6.01 g, 20 mmol) in tetrahydrofuran (180 ml) was treated at 0° C. with a 1 M solution of BH3*THF in tetrahydrofuran (49.8 ml, 49.8 mmol). The cooling bath was removed and the reaction mixture stirred at ambient temperature for 16 h. Careful quenching with MeOH and ice water, twofold extraction with AcOEt, washing with ice water/brine 1/1, drying over magnesium sulfate, and evaporation of the solvent left a crude product which was refluxed for 30 min in MeOH to liberate quantitatively the free alcohol. The solvent was evaporated in vacuo and the residue was purified by column chromatography (silica gel, dichloromethane/MeOH) to yield 5.68 g (20 mmol, 99%) of the title compound as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235572B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-b67eaf779c8842e9b4efb23589e28b78 |
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| Source note | uspto-grants-2007_06 |
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