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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254875Generated: October 26, 2026

Hydrochloric Acid → (2-Chloro-4-methanesulfonyl-phenyl)-methanol

https://huagongshe.com/reaction/1254875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Chloro-4-(methylsulfonyl)benzaldehydeHCID 2761084—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product(2-Chloro-4-methanesulfonyl-phenyl)-methanolHCID 42609245—

Reaction Steps

To a stirred dispersion of 2-chloro-4-methanesulfonyl-benzaldehyde (25 g, 0.11 mol) in absolute ethanol (120 ml) is added sodium borohydride (4.6 g, 0.12 mol) whilst cooling with an ice-bath to maintain room temperature. After stirring at room temperature for 3 hours, the reaction mixture is poured carefully onto ice-water (600 ml) and acidified to pH 1-2 with 1N HCl. The resulting suspension is extracted with ethyl acetate (400 ml) and the organic portions are combined, washed with brine, dried (MgSO4) and concentrated in vacuo. The resulting crude product is dried in a vacuum oven at 40° C. overnight to yield the titled product which is used crude in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455645B2
Source datasetuspto-grants-2013_06
ORD IDord-7dac84d079a34844b7151500a080a60b
Source noteuspto-grants-2013_06