Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251425Generated: October 26, 2026

Potassium Carbonate → Ethyl 1-benzyl-4-(4-methoxyphenyl)sulfonylpiperidine-4-carboxylate

https://huagongshe.com/reaction/1251425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant18-Crown-6HCID 28557—
Reactant2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl esterHCID 1482372—
ReactantN,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
SolventAcetoneHCID 180—
ProductEthyl 1-benzyl-4-(4-methoxyphenyl)sulfonylpiperidine-4-carboxylateHCID 3695010—

Reaction Steps

To a stirred solution of bis-(2-chloro-ethyl)-benzyl amine hydrochloride (6.6 g, 24.7 mmol), 18-Crown-6 (500 mg), and anhydrous K2CO3 (30 gm, excess) in dry acetone (250 ml), (4-methoxy-phenylsulfonyl)-acetic acid ethyl ester (6.12 gm, 24 mmol) was added in a round bottom flask and the reaction mixture was heated at reflux for 16 hours with good stirring. At the end, the reaction mixture was allowed to cool and the potassium salts were filtered off and the reaction mixture was concentrated. The residue was extracted with chloroform and washed with H2O. The organic layer was further washed well with water, dried over MgSO4, filtered and concentrated. The dark brown reaction mixture was purified by silica gel column chromatography by eluting it with 30% ethylacetate:hexane and the product 4-(4-Methoxy-benzenesulfonyl)-1-benzyl-piperidine-4-carboxylic acid ethyl ester was isolated as Brown oil. Yield: 6.0 g, 60%; MS: 418 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342508B1
Source datasetuspto-grants-2002_01
ORD IDord-6b71cae8b09e45df93390ea220a9e688
Source noteuspto-grants-2002_01