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HRID 565333作成日:2026年10月25日

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

https://huagongshe.com/reaction/565333

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 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06172057B2
出典データセットuspto-grants-2001_01
ORD IDord-008f15543b554f6484cd973c46fd09e3
出典メモuspto-grants-2001_01