Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
Reactant(5-Bromo-2-chloro-phenyl)-[4-(trifluoromethoxy)phenyl]methanoneHCID 86685137—
SolventMeOH tetrahydrofuranHCID 21899815—
Product(5-Bromo-2-chloro-phenyl)-[4-(trifluoromethoxy)phenyl]methanolHCID 58178526100.8%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394329B2
Source datasetuspto-grants-2016_07
ORD IDord-20269d73960e4f6b956bf7162cd0233e
Source noteuspto-grants-2016_07