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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380166Generated: November 1, 2026

Tetrahydrofuran → 4-Hydroxy-4'-(1-hydroxyethyl)biphenyl

https://huagongshe.com/reaction/2380166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Methylcarbonyloxy-4'-hydroxybiphenylHCID 14438409—
SolventMethanolHCID 887—
Product4-Hydroxy-4'-(1-hydroxyethyl)biphenylHCID 1393080092.9%

Reaction Steps

A solution containing 4-acetoxy-4'-hydroxy-1,1'-biphenyl from part A (5.0 g, 23.6 mmol) in methanol (500 mL) and tetrahydrofuran (30 mL) is treated with sodium borohydride (0.9 g, 23.8 mmol) in portions over 30 minutes at room temperature. After 2 hours, the reaction mixture is concentrated under reduced pressure, diluted with water (400 mL), acidified with 2N HCl and extracted with ethyl acetate. The organic layer is washed with water and brine, dried over MgSO4 and concentrated to a solid residue. Crystallization of the solid from ethyl acetate gives 4.7 g (92.9%) of the title compound, m.p. 159°-160° C.; MS (El m/z): 214 (M)+ and 199 (b.p. M-CH3)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364944
Source datasetuspto-grants-1994_11
ORD IDord-c862cfaf2d8e4603b188723b52d51107
Source noteuspto-grants-1994_11