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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 866056생성일: 2026년 10월 26일

Ethyl 4-piperidinecarboxylate → ethyl N-[4-(2-propen-1-yloxy)phenylmethyl]piperidin-4-ylcarboxylate

https://huagongshe.com/reaction/866056

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 4-piperidinecarboxylateHCID 70770—
반응물4-(Allyloxy)benzaldehydeHCID 95942—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물ethyl N-[4-(2-propen-1-yloxy)phenylmethyl]piperidin-4-ylcarboxylateHCID 1904093498.9%

반응 단계

The reaction conditions taught by A. E. Moormann, Syn. Comm., 23(6), 789-795 (1993) were used in the following preparation. To a stirred solution of 4.8 grams (0.030 mole) of ethyl piperidin-4-ylcarboxylate and 4.9 grams (0.030 mole) of 4-(2-propen-1-yloxy)benzaldehyde in 50 mL of ethanol was added 3.8 mL (0.030 mole) of borane-pyridine complex. Upon completion of addition, the reaction mixture was stirred at ambient temperature for about 18 hours. The reaction mixture was then taken up in water and extracted with methylene chloride. The organic layer was washed with water and dried with magnesium sulfate. The mixture was filtered and the filtrate concentrated under reduced pressure, yielding 9.0 grams of ethyl N-[4-(2-propen-1-yloxy)phenylmethyl]piperidin-4-ylcarboxylate. The NMR spectrum was consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05569664
출처 데이터셋uspto-grants-1996_10
ORD IDord-3e0acf32c1dd480bbf13d4c2f7d72993
출처 메모uspto-grants-1996_10