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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015696Generated: October 31, 2026

Lithium borohydride → (5-Chloro-2-(methylsulfonyl)phenyl)methanol

https://huagongshe.com/reaction/1015696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantMethyl 5-chloro-2-(methylsulfonyl)benzoateHCID 66877882—
Solvent2-(Oxolan-2-yl)ethan-1-olHCID 11989572—
Product(5-Chloro-2-(methylsulfonyl)phenyl)methanolHCID 6688598789.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

(Step 2) To a solution of methyl 5-chloro-2-(methylsulfonyl)benzoate obtained in Step 1 (2.65 g) in tetrahydrofuran-ethanol (50 ml+5 ml) was added lithium borohydride (348 mg) at 0° C. The mixture was stirred at 60° C. for 2 hr, treated with ice, and extracted with ethyl acetate. The extract was washed successively with 1N hydrochloric acid and saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=2:1) to give [5-chloro-2-(methylsulfonyl)phenyl]methanol (2.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985862B2
Source datasetuspto-grants-2011_07
ORD IDord-90ddb0e3b8184d4b967e30e80fe09290
Source noteuspto-grants-2011_07