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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 460657생성일: 2026년 10월 24일

4-(Naphthalen-2-yl)piperidine → (S)-alpha-(2'-(2-Hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)benzylidene)-gamma-butyrolactone

https://huagongshe.com/ko/reaction/460657

반응식

참여 물질

역할이름HCID투입량
반응물4-(Naphthalen-2-yl)piperidineHCID 22029264—
반응물(S)-alpha-(2'-(2,3-epoxypropan-1-yloxy)benzylidene)-gamma-butyrolactoneHCID 86585643—
용매EthanolHCID 702—
생성물(S)-alpha-(2'-(2-Hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)benzylidene)-gamma-butyrolactoneHCID 6949791353.8%

반응 단계

(S)-α-(2′-(2,3-epoxypropan-1-yloxy)benzylidene)-γ-butyrolactone (50 g) and 4-(naphthalen-2-yl)piperidine (43 g) were dissolved in ethanol (500 ml) and the mixture was refluxed under heating for 2 hr. After cooling, the solvent was evaporated under reduced pressure and the obtained crystals were collected by filtration. The crystals were recrystallized once from acetonitrile and once from a mixed solvent of ethyl acetate and ethanol to give the title compound (50 g), melting point 138–140° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196199B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-857f9eddc4a9439095e53212e9b9fd2f
출처 메모uspto-grants-2007_03