HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055532Generated: November 1, 2026
Sodium → (5-Bromo-2-chloro-phenyl)-[4-(trifluoromethoxy)phenyl]methanol
https://huagongshe.com/reaction/1055532
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | (5-Bromo-2-chloro-phenyl)-[4-(trifluoromethoxy)phenyl]methanone | HCID 86685137 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | (5-Bromo-2-chloro-phenyl)-[4-(trifluoromethoxy)phenyl]methanol | HCID 58178526 | 100.8% |
Reaction Steps
To the solution of (5-bromo-2-chloro-phenyl)-[4-(trifluoromethoxy)phenyl]methanone 15e (5.0 g, 13.0 mmol) in a dry tetrahydrofuran/methanol mixture (v/v=1/1, 20 mL) was added sodium brohydride (0.98 g, 26.0 mmol) in portions at 0° C. After the addition, the mixture was stirred at 0° C. for 40 min. The reaction mixture was quenched with water (5 mL) and extracted with ethyl acetate (50 mL). The water layer was extracted with ethyl acetate (30 mL×2). The combined organic layers were washed with saturated brine (30 mL×2), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to give the title compound 15f as pale yellow oil (5.0 g, 99.5%). This material was not further purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394329B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-20269d73960e4f6b956bf7162cd0233e |
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| Source note | uspto-grants-2016_07 |
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