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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715563Generated: October 25, 2026

4-Phenylcyclohexanone → HCID 178521548, compound

https://huagongshe.com/reaction/715563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenylcyclohexanoneHCID 78605—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 178521548HCID 178521548—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Phenylcyclohexanone (4 g) is dissolved under argon in MeOH (25 mL), cooled to 0° C. and treated portionwise with NaBH4 (900 mg). The mixture is stirred for 12 hours while warming to room temperature. The mixture is concentrated and then treated dropwise with water (10 mL). Then concentrated hydrochloric acid (8 mL) is added dropwise. The mixture is extracted with ethylacetate and the organic phase is washed with brine and dried (Na2SO4). The solvents are evaporated and the residue is crystallized from cyclohexane to give the title compound. TLC: rf=0.52 (silicagel, dichloromethane/ethanol 19:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187477B2
Source datasetuspto-grants-2015_11
ORD IDord-9d9563f3f3a34bc8896e1af91df73b00
Source noteuspto-grants-2015_11