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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875255Generated: October 29, 2026

Sodium borohydride → 2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanol

https://huagongshe.com/reaction/875255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanoneHCID 86657994—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanolHCID 6721250770%

Reaction Steps

A stirred solution of 2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanone (0.33 g, 1.28 mmol, 88.4% A) in ethanol (2.5 ml) was cooled to 0° C. under nitrogen. NaBH4 (60.1 mg, 1.59 mmol) was added to the solution and the reaction mixture stirred for 2 hours. After checking by GPC that the starting product had disappeared, the mixture was diluted with demineralized water (7 ml) and dichloromethane (7 ml) and the phases separated. The organic layer was dried over anhydrous sodium sulphate, filtered and concentrated under vacuum to give crude 2-Chloro-1-(6-fluoro-1-benzopyran-2-yl)-ethanol as a mixture of diastereoisomers 54:46 (0.30 g, 70% yield, 67.9% A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981127B2
Source datasetuspto-grants-2015_03
ORD IDord-be09a0a66b9d45849aaa9811caf8eb00
Source noteuspto-grants-2015_03