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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 343498생성일: 2026년 10월 26일

Benzyl Bromide → 1-Benzyl-4-cyano-4-phenylpiperidine

https://huagongshe.com/reaction/343498

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물4-Phenylpiperidine-4-carbonitrile hydrochlorideHCID 3084973—
용매Oxolane--water (1/1)HCID 21881883—
생성물1-Benzyl-4-cyano-4-phenylpiperidineHCID 191408—

반응 단계

Alternately, combine 4-phenyl-4-cyano-piperidine hydrochloric acid salt (10 g, 44.9 mmol), benzyl bromide (5.4 mL, 45.4 mmol), and potassium carbonate (25.2g, 182.3 mmol) in tetrahydrofuran/water (80 mL/20 mL). After 18 hours, partition the reaction mixture between water and dichloromethane. Separate The organic layer and extract with water, dry over MgSO4, filter and evaporate invacuo to give a residue. Recrystallize the residue from hexane to give 1-benzyl-4-phenyl-4-cyanopiperidine as a solid: mp; 73°-74° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05861417
출처 데이터셋uspto-grants-1999_01
ORD IDord-6af9594e2cda42c1a919923860343293
출처 메모uspto-grants-1999_01