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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 565333생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물18-Crown-6HCID 28557—
반응물2-[(4-Methoxyphenyl)sulfonyl]acetic acid ethyl esterHCID 1482372—
반응물N,N-Bis(2-chloroethyl)benzylamine hydrochlorideHCID 2777881—
용매AcetoneHCID 180—
생성물Ethyl 1-benzyl-4-(4-methoxyphenyl)sulfonylpiperidine-4-carboxylateHCID 3695010—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06172057B2
출처 데이터셋uspto-grants-2001_01
ORD IDord-008f15543b554f6484cd973c46fd09e3
출처 메모uspto-grants-2001_01