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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014007Generated: October 31, 2026

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

https://huagongshe.com/reaction/1014007

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 numberUS07982044B2
Source datasetuspto-grants-2011_07
ORD IDord-4627b0ca70a0458fb5d4e0ad19cfadce
Source noteuspto-grants-2011_07