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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423262Generated: October 31, 2026

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

https://huagongshe.com/reaction/2423262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-chloro-1-(6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanoneHCID 16755387—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Chloro-1-(6-fluorochroman-2-yl)ethanolHCID 6724312470%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution under stirring of 2-chloro-1-(6-fluoro-3,4-dihydro-2H-chromen-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 that the starting product had disappeared by GC, the mixture was diluted with demi water (7 ml) and dichloromethane (7 ml) and the phases separated. The organic stratum was dried under anhydrous sodium sulphate, filtered and concentrated under vacuum to give raw 2-chloro-1-(6-fluoro-3,4-dihydro-2H-chromen-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 numberUS07960572B2
Source datasetuspto-grants-2011_06
ORD IDord-63c947e7ab5145d2ab3af2f0f34bffe0
Source noteuspto-grants-2011_06