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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748523Generated: November 1, 2026

Water → HCID 178521544, compound

https://huagongshe.com/reaction/1748523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(5-Bromopyridin-2-yl)cyclohexanoneHCID 86692465—
SolventEthanolHCID 702—
ProductHCID 178521544HCID 178521544—
ProductHCID 178521545HCID 178521545—

Reaction Steps

Sodium borohydride (4.58 g) was added under ice cooling to a solution of 4-(5-bromopyridin-2-yl)cyclohexanone (7.9 g) in ethanol (120 ml), and stirred at the same temperature for an hour. After completion of the reaction, water was added under ice cooling, the organic solvent was evaporated and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated. The resulting residue was purified with silica gel column chromatography (n-hexane/ethyl acetate) to give trans-4-(5-bromopyridin-2-yl)cyclohexanol (4.94 g) as a white solid, and cis-4-(5-bromopyridin-2-yl)cyclohexanol (1.16 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-a6dceb590c3243769660125af2ee1788
Source noteuspto-grants-2015_10