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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803631Generated: November 1, 2026

Sodium borohydride → HCID 71170040, compound

https://huagongshe.com/reaction/1803631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(Furan-2-yl)-2-(3-benzyloxyphenyl)ethan-1-oneHCID 71170035—
SolventMethanolHCID 887—
ProductHCID 71170040HCID 71170040—

Reaction Steps

1-(Furan-2-yl)-2-(3-benzyloxyphenyl)ethan-1-one (4 kg, 13.69 mol) was dissolved in MeOH (35 L), and NaBH4 (520 g, 13.75 mol) was slowly added to the solution at 5° C. After the reaction was completed, the solution was quenched with H2O, and the MeOH was evaporated. The residue was extracted with EtOAc and the organic layer was washed with brine, dried over MgSO4, and evaporated to give the 1-(furan-2-yl)-2-(3-benzyloxyphenyl)ethan-1-ol as yellow oil: 3.97 kg (crude yield: 98%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350090B1
Source datasetuspto-grants-2013_01
ORD IDord-b67e4372c76d47dfb1b43c3c7b854972
Source noteuspto-grants-2013_01