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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845144Generated: November 1, 2026

Sodium borohydride → 1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanol

https://huagongshe.com/reaction/1845144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanoneHCID 58188228—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanolHCID 58187981—

Reaction Steps

A round bottom flask was charged with 1-(4-chloro-3-(methylsulfonyl)phenyl)ethanone (12.0 g, 50.0 mmol) and tetrahydrofuran (100 mL) at 0° C. Sodium borohydride (3.7 g, 100 mmol) was added in portions and the reaction was stirred for 12 h at room temperature. The reaction was quenched with ice and extracted with MTBE. The organic solvents were removed under reduced pressure and the residue was purified by flash chromatography to get the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946439B2
Source datasetuspto-grants-2015_02
ORD IDord-04c9c3ac5a06490b9bbfb2cb5b8cfa06
Source noteuspto-grants-2015_02