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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980102Generated: October 30, 2026

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

https://huagongshe.com/reaction/1980102

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 numberUS04485112
Source datasetuspto-grants-1984_11
ORD IDord-3b7de48b68794ecca5280b1b0fe71902
Source noteuspto-grants-1984_11