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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046546Generated: November 1, 2026

Sodium borohydride → 6-Bromo-2,3-dihydro-1-benzofuran-3-ol

https://huagongshe.com/reaction/2046546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant6-Bromo-1-benzofuran-3(2H)-oneHCID 44119520—
SolventMethanolHCID 887—
Product6-Bromo-2,3-dihydro-1-benzofuran-3-olHCID 6829674192%

Reaction Steps

To a solution of 6-bromo-benzofuran-3-one (10.5 g, 49.28 mmol) in methanol (100 ml) was added NaBH4 (2.37 g, 64.07 mmol) at 0° C. The reaction mixture was then stirred for 2 hours at room temperature. It was subsequently quenched with saturated ammonium chloride solution (50 ml) and extracted twice with ethyl acetate (2×50 ml). The combined organic phases were dried over Na2SO4 and evaporated under reduced pressure to give 9.75 g (92%) of the title compound as colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592426B2
Source datasetuspto-grants-2013_11
ORD IDord-8f7788a8c8d54cbf90a57bb66c3784ec
Source noteuspto-grants-2013_11