Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113187Generated: October 30, 2026

Water → 4'-(2-Benzylbenzofuran-3-yl)biphenyl-4-methanol

https://huagongshe.com/reaction/2113187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant4'-(2-Benzylbenzofuran-3-yl)biphenyl-4-carbaldehydeHCID 59855511—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product4'-(2-Benzylbenzofuran-3-yl)biphenyl-4-methanolHCID 6881995199.7%

Reaction Steps

To a solution of 4′-(2-benzylbenzofuran-3-yl)biphenyl-4-carbaldehyde (5.0 g, 12.9 mmol) in ethanol (100 mL) and tetrahydrofuran (25 mL) was added sodium borohydride (980 mg, 25.8 mmol) as a solid in 3 portions. The reaction was stirred at room temperature for 1 hour (TLC control) and then poured into water (100 mL) and extracted with diethyl ether (3×100 mL). The combined extract was washed with water, brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to afford the title compound as a white solid (5.02 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524878B2
Source datasetuspto-grants-2009_04
ORD IDord-847cf8162f654f989573b33233f75225
Source noteuspto-grants-2009_04