Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 565333Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/565333

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt18-Crown-6HCID 28557—
Edukt2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl esterHCID 1482372—
EduktN,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
LösungsmittelAcetoneHCID 180—
ProduktEthyl 1-benzyl-4-(4-methoxyphenyl)sulfonylpiperidine-4-carboxylateHCID 3695010—

Reaktionsschritte

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 coumn 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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06172057B2
Quelldatensatzuspto-grants-2001_01
ORD IDord-008f15543b554f6484cd973c46fd09e3
Quellennotizuspto-grants-2001_01