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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709208Generated: October 30, 2026

Sodium borohydride → 4-(4-Bromophenoxy)cyclohexanol

https://huagongshe.com/reaction/709208

Reaction equation

Participants

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

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 00° C. and quenched by the addition of 1 N HCl (aq). The reaction was concentrated and the resulting residue was partitioned between ether and 1 N HCl (aq). The layers were separated, the organic layer was washed with water then dried (Na2SO4), filtered and concentrated. Purification on an Analogix SF15-12 g 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 numberUS09180123B2
Source datasetuspto-grants-2015_11
ORD IDord-c04ad4b26c8240ef8feb0cef81da6354
Source noteuspto-grants-2015_11