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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413675생성일: 2026년 10월 24일

Methyl Ethyl Ketone → (R)-1-(4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-benzyl)-3-piperidinecarboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/413675

반응식

참여 물질

역할이름HCID투입량
반응물Methyl Ethyl KetoneHCID 6569—
반응물Potassium CarbonateHCID 11430—
반응물Iodide IonHCID 30165—
반응물ethyl (3R)-piperidine-3-carboxylateHCID 185582—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물(R)-1-(4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-benzyl)-3-piperidinecarboxylic acid ethyl esterHCID 5383576977%

반응 조건

온도50 °C

반응 단계

A mixture of the above iodide (1.80 g, 0.0044 mol), (R)-3-piperidinecarboxylic acid ethyl ester (0.69 g, 0.0044 mol) and anhydrous potassium carbonate (1.82 g, 0.0132 mol) in 2-butanone (30 ml) was heated to 50° C. for 6 h. After cooling, the mixture was diluted with ether (50 ml) and water (50 ml) and the phases were separated. The organic phase was washed with water (30 ml) and dried (MgSO4). The solvent was evaporated in vacuo and the oily residue (2.1 g) was purified by gradient column chromatography on silica gel (40 g) using benzene and ethyl acetate as eluents. The benzene/ethyl acetate (9:1) fraction afforded 1.50 g (77%) of (R)-1-(4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-benzyl)-3-piperidinecarboxylic acid ethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06569849B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-58df006fae444ce5a99798597a2d0096
출처 메모uspto-grants-2003_05