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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1900250생성일: 2026년 10월 25일

Methanol → 4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-1-methyl-1,2,5,6-tetrahydropyridine

https://huagongshe.com/reaction/1900250

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-methylpiperidineHCID 168897—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-1-methyl-1,2,5,6-tetrahydropyridineHCID 2147413394%

반응 조건

온도-78 °C

반응 단계

Dissolved 4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-1-methylpiperidine (12 g, 0.042 mol) in 250 mL of dry THF. Cooled to -78° C. under a nitrogen atmosphere. Added n-butyl lithium (18 mL of 2.5M in hexane) dropwise via addition funnel. Maintain temperature at 0° C. for 1 hour then recooled to -78° C. Added 21 mL of dry methanol, and let warm to room temperature. Added saturated NH4Cl, and extracted with THF. Dried combined organic extracts with MgSO4, filtered, and evaporated to give 11.3 g (94% yield) of 4-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-yl)-1-methyl-1,2,5,6-tetrahydropyridine as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05574173
출처 데이터셋uspto-grants-1996_11
ORD IDord-19a91169cece42e8b3db6a59a930f340
출처 메모uspto-grants-1996_11