Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263521Generated: October 28, 2026

Sodium borohydride → HCID 178455058, compound

https://huagongshe.com/reaction/1263521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(2,4-Bis{[tert-butyl(dimethyl)silyl]oxy}phenyl)cyclohexan-1-oneHCID 22337814—
SolventEthanolHCID 702—
ProductHCID 178455058HCID 17845505835%

Reaction Steps

Sodium borohydride (164 mg) was added to a stirred solution of 4-(2,4-bis{(tert-butyl(dimethyl)silyl]oxy}phenyl)cyclohexanone (1.57 g) in ethanol (50 ml) at 0° C. After 18 hr at room temperature, the mixture was partitioned between 2M HCl (20 ml), water (40 ml) and ethyl acetate (50 ml) and the aqueous layer was re-extracted with ethyl acetate (2×50 ml). The combined organic extracts were washed with brine (40 ml), dried over magnesium sulfate and evaporated in vacuo. The residue was purified using flash column chromatography (SiO2, ethyl acetate/petrol, 3:17 v/v) to give the trans-title compound as a white solid (546 mg, 35%), and the cis-title compound as a white solid (83 mg, 5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541473B2
Source datasetuspto-grants-2003_04
ORD IDord-f9540e423fb44a918d93cb15f52e5778
Source noteuspto-grants-2003_04