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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260664Generated: October 26, 2026

Hydrochloric Acid → 3-Fluoro-4-(methylsulphonyl)benzyl alcohol

https://huagongshe.com/reaction/1260664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Fluoro-4-methanesulfonylbenzaldehydeHCID 21251732—
SolventEthanolHCID 702—
Product3-Fluoro-4-(methylsulphonyl)benzyl alcoholHCID 67219085—

Reaction Steps

To an ice-cooled suspension of 3-fluoro-4-methanesulfonyl-benzaldehyde (1.3 g, 6.44 mmol) in ethanol (5 ml) under an inert atmosphere of Argon is added sodium borohydride (0.275 g, 7.27 mmol) portionwise over 2-3 minutes. After stirring for 4 hours, the reaction mixture is poured carefully onto ice-cold water and acidified to pH 1 using 1M HCl. The product is extracted into ethyl acetate (80 ml) and this organic portion is washed with brine, dried over MgSO4 and the solvent is removed in vacuo to give an oil which solidifies on drying to yield the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470848B2
Source datasetuspto-grants-2013_06
ORD IDord-ba3b1e92f2a84578939e72dbfe91ed03
Source noteuspto-grants-2013_06