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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013950Generated: October 31, 2026

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

https://huagongshe.com/reaction/1013950

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 numberUS07982044B2
Source datasetuspto-grants-2011_07
ORD IDord-25b325d19ca849cca994a74d7d315fb4
Source noteuspto-grants-2011_07