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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1797036생성일: 2026년 10월 25일

2-Phenylpropionic acid → 1-(4-Hydroxypiperidin-1-yl)-3-phenylpropan-1-one

https://huagongshe.com/reaction/1797036

반응식

참여 물질

역할이름HCID투입량
반응물2-Phenylpropionic acidHCID 10296—
반응물Sodium HydroxideHCID 14798—
반응물Benzenepropanoyl chlorideHCID 64801—
반응물Piperidin-4-olHCID 79341—
용매TolueneHCID 1140—
생성물1-(4-Hydroxypiperidin-1-yl)-3-phenylpropan-1-oneHCID 2217516239%

반응 단계

This amine was synthesized in accordance with the method of Scheme 37. To 4 g (40 mmol) of 4-hydroxypiperidine in 20 mL of toluene was added phenylpropionyl chloride (derived from 6 g (40 mmol) of phenylpropionic acid in excess thionyl chloride). To the mixture was added excess 2N aqueous NaOH. After stirring 24 hours, the toluene layer was discarded and the aqueous phase was extracted with CH2Cl2, dried, and evaporated under vacuum to give 3.63 g (39%) of 1-(3-phenylpropionyl)-4-hydroxypiperidine (134). GC/MS indicated 100% purity with a molecular ion of 233.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07034035B2
출처 데이터셋uspto-grants-2006_04
ORD IDord-6bbe7f7bc04640a7a2e7ea520760f651
출처 메모uspto-grants-2006_04