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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895902Generated: October 30, 2026

Sodium borohydride → 1-(3-(Trifluoromethyl)phenylsulfonyl)piperidin-4-ol

https://huagongshe.com/reaction/1895902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(3-(Trifluoromethyl)phenylsulfonyl)piperidin-4-oneHCID 10709847—
SolventMethanolHCID 887—
Product1-(3-(Trifluoromethyl)phenylsulfonyl)piperidin-4-olHCID 372926284.1%

Reaction Steps

NaBH4 (180 mg, 4.74 mmol) was added to a solution of 1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-one (2.56 g, 8.34 mmol) in methanol (15 ml) at 0° C., and stirred at room temperature for 1 hour. The reaction was quenched with H2O (50 ml) and extracted with ethyl acetate (20 ml×2). The combined organic phase was washed with H2O (20 ml×2) and brine (20 ml×2), dried over Na2SO4 and concentrated in vacuo to give 1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-ol (2.17 g, 84%) as a white solid: LCMS: 310 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518934B2
Source datasetuspto-grants-2013_08
ORD IDord-b6fd2e18d3e54e1c939e1c9fa01842ae
Source noteuspto-grants-2013_08