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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223369생성일: 2026년 10월 24일

Propyltriphenylphosphonium bromide → 1-Carbobenzoxy-4-(1-butylidene)piperidine

https://huagongshe.com/ko/reaction/223369

반응식

참여 물질

역할이름HCID투입량
반응물Propyltriphenylphosphonium bromideHCID 80374—
반응물Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-Carbobenzoxy-4-(1-butylidene)piperidineHCID 20522020—

반응 단계

Butyl lithium (44 ml of 1.6 M in hexane) was added slowly to a stirred suspension of 27 g of (n-propyl)triphenylphosphonium bromide in 350 ml of tetrahydrofuran and the resulting solution was refluxed for 1 hour. The mixture was cooled in an ice bath and 18 g of N-carbobenzyloxy-4-piperidone was added. After stirring at room temperature of 0.5 hour, the solution was refluxed for 2 hours. The cooled mixture was concentrated under reduced pressure, partitioned between ether and water, and the ether layer was dried (sodium sulfate) and evaporated. The residue was filtered through silica gel with 20% ethyl acetate-hexane to give 10 g of 1-carbobenzoxy-4-(1-butylidene)piperidine as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04353901
출처 데이터셋uspto-grants-1982_10
ORD IDord-f068b0d416624defa98b220467acb3f2
출처 메모uspto-grants-1982_10