돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2225517생성일: 2026년 10월 26일

Sodium Chloride → 1-(4-Hydroxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/2225517

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Ammonium formateHCID 2723923—
반응물Allyl 1-(4-allyloxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylateHCID 53899198—
촉매HCID 178418476HCID 178418476—
용매TetrahydrofuranHCID 8028—
생성물1-(4-Hydroxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylic acidHCID 53657751125.1%

반응 단계

0.4 g of bis(triphenylphosphine)palladium dichloride and 5 g of ammonium formate were added to a solution of 1.1 g of allyl 1-(4-allyloxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylate (Example 67) in 100 ml of THF. Under an argon stream, the solution was reacted for hours, while it was refluxed. After reaction, 150 ml of an aqueous sodium chloride solution was added to the reaction solution. The solution was extracted three times with 50 ml of ethyl acetate. The organic layer obtained was washed three times with an aqueous sodium chloride solution and dried over magnesium sulfate. Thereafter, the solvent was removed in vacuo, yielding 1.1 g of 1-(4-hydroxy-3-methoxycinnamoyl)-4-methylpiperidine-4-carboxylic acid (a compound of the present invention) as a pale yellow oil, which had the following physiochemical properties:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05344845
출처 데이터셋uspto-grants-1994_09
ORD IDord-e22296aa17354f3abaa1c0380a77b429
출처 메모uspto-grants-1994_09