HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203012Generated: October 30, 2026
Methanol → 5-(Trifluoromethyl)-3-thiophenemethanol
https://huagongshe.com/reaction/2203012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 5-(trifluoromethyl)thiophene-3-carboxylate | HCID 89690311 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Trifluoromethyl)-3-thiophenemethanol | HCID 19957393 | 99.1% |
Reaction Steps
To a solution of methyl 5-(trifluoromethyl)thiophene-3-carboxylate (523 mg) in THF (1 ml)-MeOH (1 ml) was added NaBH4 (2.2 g) at room temperature, and the reaction mixture was stirred at 60° C. for 3 h. The reaction mixture was quenched with water, and extracted with EtOAc. The extract was washed with brine, dried over MgSO4, concentrated and purified by silica gel column chromatography (hexane/EtOAc) to give the title compound (449 mg) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365540B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-1e2c80422bdb4179887d3c9cdb8d9899 |
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| Source note | uspto-grants-2016_06 |
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