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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034416Generated: October 30, 2026

Triethylamine → HCID 15229595, compound

https://huagongshe.com/reaction/1034416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantToluene-p-sulphonic anhydrideHCID 77773—
Reactant4-Piperidineethanol, 1-benzoyl-HCID 10421498—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 15229595HCID 1522959589%

Reaction Steps

A solution of p-toluene sulfonic anhydride (6.0 g, 18 mmol) in dichloromethane (50 mL) was added dropwise over 1 hour to a room temperature solution of 1-benzoyl-4-hydroxyethylpiperidine (4.3 g, 18 mmol) and dry triethylamine (2.8 mL, 2 mmol) in dichloromethane. After 2 hours, the mixture was diluted with ethyl acetate (500 mL) and extracted successively with H2O (2 ×100 mL), cold 0.1 M aqueous HCl (100 mL), saturated aqueous NaHCO3 (100 mL), and brine (50 mL), dried (MgSO4), filtered, and concentrated in vacuo. The crude product was purified by chromatography on silica gel, eluting with ethyl acetate, and concentrated to yield a crystalline solid (6.2 g, 89%) which melted at 81°-83° C. Analysis: Calculated for C21H25NO4S: C,65.09; H,6.50; N,3.61; S,8.27; found: C.,65.31; H,6.74; N,3.41; S,8.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05317024
Source datasetuspto-grants-1994_05
ORD IDord-876f9b564e044606a553d54df876f9f5
Source noteuspto-grants-1994_05