戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2305874作成日:2026年10月27日

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

https://huagongshe.com/reaction/2305874

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物18-Crown-6HCID 28557—
反応物2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl esterHCID 1482372—
反応物N,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
溶媒AcetoneHCID 180—
生成物Ethyl 1-benzyl-4-(4-methoxyphenyl)sulfonylpiperidine-4-carboxylateHCID 3695010—

反応手順

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 gmn, 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 stirig. At the end, the reaction miixture 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 furher washed well with water, dried over MgSO4, fitered and concentrated. The dark brown reaction mixture was purified by silica gel couinn chromatography by eluting it with 30% ethylace tate: 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06441023B1
出典データセットuspto-grants-2002_08
ORD IDord-581ebd412bbb480e9bf355386d9c539a
出典メモuspto-grants-2002_08