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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475818Generated: November 1, 2026

Sodium borohydride → 4-(4-Bromophenoxy)cyclohexanol

https://huagongshe.com/reaction/1475818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(4-Bromophenoxy)cyclohexanoneHCID 67248883—
SolventEthanolHCID 702—
Product4-(4-Bromophenoxy)cyclohexanolHCID 6724967472%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium borohydride (77.3 mg, 2.04 mmol) was added to a solution of 4-(4-bromophenoxy)cyclohexanone (500 mg, 1.86 mmol) in ethanol (10 mL) at room temperature. After 20 minutes the reaction was cooled to 0° C. and quenched by the addition of 1N HCl (aq). The reaction was concentrated and the resulting residue was partitioned between ether and 1N HCl (aq). The layers were separated, the organic layer was washed with water then dried (Na2SO4), filtered and concentrated. Purification on an Analogix SF15-12g column (hexanes/ethyl acetate=8:2) afforded the title compound as a white solid (360 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018384B2
Source datasetuspto-grants-2015_04
ORD IDord-1e63593ca7ed4c23a289b17dcb26f940
Source noteuspto-grants-2015_04