HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480484Generated: October 30, 2026
3-Bromo-5-(trifluoromethyl)benzoic acid → [3-Bromo-5-(trifluoromethyl)phenyl]methanol
https://huagongshe.com/reaction/1480484
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromo-5-(trifluoromethyl)benzoic acid | HCID 11086788 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [3-Bromo-5-(trifluoromethyl)phenyl]methanol | HCID 29919767 | — |
Reaction Steps
To a stirred solution of 3-bromo-5-(trifluoromethyl)benzoic acid (1 g, 3.72 mmol) in THF (5 ml) at −78° C. with stirring under nitrogen was added dropwise over 10 mins borane tetrahydrofuran complex 1M in THF (18.59 ml, 18.59 mmol) and then the reaction mixture was warmed to RT over 20 hours. The reaction mixture was cooled in an ice/water bath and quenched dropwise with MeOH (10 ml) followed by 1M HCl until effervescence ceased. Water was added and stirred at RT for 30 mins. THF was removed under reduced pressure, and the compound extracted into EtOAc. The organic portion was dried over MgSO4, filtered and concentrated under reduced pressure. Purification was carried out by chromatography on silica using 0-50% EtOAc in Hexanes as eluent to afford the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409895B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-2bafdf9c025d4e3bb15e6a9f4c395e29 |
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| Source note | uspto-grants-2016_08 |
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