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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416670Generated: October 30, 2026

Water → HCID 12136657, compound

https://huagongshe.com/reaction/2416670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 12136656HCID 12136656—
SolventMethanolHCID 887—
ProductHCID 12136657HCID 1213665788.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 1-{4-[5-(4-chloro-benzenesulfonyl)2-methoxyphenyl]piperidin-1-yl}-2,2,2-trifluoro-ethanone (31) (77 mg) in methanol (2 mL), a solution of 6N NaOH (0.5 mL) was added. After stirring at 80° C. for 10 min, water was added (10 ml) and the mixture was extracted into ethyl acetate (20 ml). The organic phase was dried (Na2SO4) and concentrated in vacuo to give 4-[5-(4-chloro-benzenesulfonyl)2methoxy-phenyl] piperidine (301) as a white solid (0.054 g ), MS, MH+ 365. The hydrochloride salt was prepared from ethanol-hydrogen chloride, m.p. 235.5-236.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825202B2
Source datasetuspto-grants-2004_11
ORD IDord-28885d7c0e984811aa161152fd130638
Source noteuspto-grants-2004_11