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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267302Generated: October 30, 2026

Piperidine → 1-[4-(1-Piperidinylsulfonyl)phenyl]ethanone

https://huagongshe.com/reaction/2267302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
Reactant4-Acetylbenzenesulfonyl chlorideHCID 266418—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product1-[4-(1-Piperidinylsulfonyl)phenyl]ethanoneHCID 75036494%

Reaction Steps

A mixture of 4-acetylbenzene-1-sulfonyl chloride (2 g, 9.2 mmol), piperidine (0.85 g, 10.0 mmol) and triethylamine (1.9 g, 18.4 mmol) in tetrahydrofuran (60 mL) was stirred at rt overnight. Brine (100 mL) was added and the mixture was extracted with ethyl acetate (3×100 mL). The combined organic layer was washed with brine (100 mL), dried over anhydrous sodium sulfate and filtered. Removal of solvent in vacuo gave the title compound as a white solid (2.3 g, 94%). MS (M+H)+ 268.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-56251eda20204b12bd8db97a8cd22a71
Source noteuspto-grants-2010_12