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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828807Generated: November 1, 2026

Sodium borohydride → HCID 69527632, compound

https://huagongshe.com/reaction/1828807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22058586HCID 22058586—
SolventEthanolHCID 702—
ProductHCID 69527632HCID 6952763294.6%

Reaction Steps

To a suspension of 4-((tert-butyldiphenylsiloxy)methyl)-3-chlorobenzaldehyde (3.24 g) in ethanol (32 ml) was added sodium borohydride (149 mg) under ice-cooling and the mixture was stirred at room temperature for 3 hr. The reaction mixture was concentrated to about half amount. Water was added and the resulting product was extracted twice with diisopropyl ether. The organic layers were combined, washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=5/1) to give 4-((tert-butyldiphenylsiloxy)methyl)-3-chlorobenzyl alcohol (3.08 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060721B1
Source datasetuspto-grants-2006_06
ORD IDord-27354e00d3b34f24ae97da49e0cbe085
Source noteuspto-grants-2006_06