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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507527Generated: November 4, 2026

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

https://huagongshe.com/reaction/507527

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 numberUS07786132B2
Source datasetuspto-grants-2010_08
ORD IDord-c564f21aa14b4ac3831f7dfe5253d484
Source noteuspto-grants-2010_08