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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178518Generated: October 31, 2026

4-Toluenesulfonyl chloride → HCID 89500606, compound

https://huagongshe.com/reaction/2178518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant1-[2-(2-Hydroxyethyl)phenyl]piperidin-2-oneHCID 89500266—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventDichloromethaneHCID 6344—
ProductHCID 89500606HCID 8950060688.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Dimethylaminopyridine (1.83 g, 15 mmol, 0.05 eq) and triethylamine (63.5 ml, 450 mmol, 1.5 eq) are added to a solution of 1-[2-(2-hydroxyethyl)phenyl]piperidin-2-one a2-2 (65.7 g, 300 mmol, 1 eq) in dichloromethane (250 ml) at 0° C. The mixture is stirred at 0° C. for 15 minutes, then a solution of 4-toluenesulfonyl chloride (63 g, 330 mmol, 1.1 eq) in dichloromethane (250 ml) is added dropwise. The reaction mixture is then warmed up to room temperature and stirred overnight. The reaction mixture is washed with water, 1N HCl, then dried over MgSO4, filtered and evaporated under vacuum. The residue is purified by chromatography over silicagel (gradient: CH2Cl2/MeOH from 100/0 to 98/2) to afford 99 g of 2-[2-(2-oxopiperidin-1-yl)phenyl]ethyl 4-methylbenzenesulfonate a2-3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067930B2
Source datasetuspto-grants-2015_06
ORD IDord-da7465ea43c54a2eb6e5d451daa1eb5d
Source noteuspto-grants-2015_06