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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364011Generated: November 2, 2026

(5-bromo-1-benzofuran-2-yl)(phenyl)methanone → (5-Bromo-1-benzofuran-2-yl)(phenyl)methanol

https://huagongshe.com/reaction/364011

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-bromo-1-benzofuran-2-yl)(phenyl)methanoneHCID 801609—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product(5-Bromo-1-benzofuran-2-yl)(phenyl)methanolHCID 3067860—

Reaction Steps

4 g of sodium borohydride dissolved in the minimum quantity of water are slowly added at ambient temperature to 8.5 g of 2-benzoyl-5-bromobenzofuran in 50 ml of dioxane. When the addition is finished, the mixture is kept stirring at ambient temperature for a further 3 hours. The solvent is removed under reduced pressure, the residue is redissolved in 50 ml of water, and extracted with ethyl ether. The ether phase is dried with anhydrous sodium sulphate, evaporated to dryness, and leaves a residue which on crystallising from cyclohexane has a M.P. of 56°-58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04604392
Source datasetuspto-grants-1986_08
ORD IDord-46de489a1ecf414fa6f1625c1d6f89df
Source noteuspto-grants-1986_08