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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015754Generated: October 30, 2026

Lithium borohydride → [2-(Cyclopentylsulfonyl)phenyl]methanol

https://huagongshe.com/reaction/1015754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantMethyl 2-(cyclopentylsulfonyl)benzoateHCID 66877458—
Solvent2-(Oxolan-2-yl)ethan-1-olHCID 11989572—
Product[2-(Cyclopentylsulfonyl)phenyl]methanolHCID 6687710684.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

(Step 2) To a solution of methyl 2-(cyclopentylsulfonyl)benzoate obtained in Step 1 (4.1 g) in tetrahydrofuran-ethanol (100 ml+10 ml) was added lithium borohydride (500 mg) at 0° C. The mixture was stirred at 60° C. for 3 hr, quenched with 1N hydrochloric acid, and extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and filtered. The solvent was evaporated under reduced pressure to give [2-(cyclopentylsulfonyl)phenyl]methanol (3.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985862B2
Source datasetuspto-grants-2011_07
ORD IDord-13fad13ac7e140af98a44164f2270c2d
Source noteuspto-grants-2011_07