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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22327생성일: 2026년 10월 24일

4-Phenylpiperidine → 7-methoxy-3,4-dimethyl-6-[3-(4-phenyl-1-piperidinyl)propoxy]-2H-1-benzopyran-2-one

https://huagongshe.com/ko/reaction/22327

반응식

참여 물질

역할이름HCID투입량
반응물4-PhenylpiperidineHCID 69873—
반응물FumarateHCID 5460307—
반응물6-[3-(methanesulfonyloxy)propoxy]-7-methoxy-3,4-dimethyl-2H-1-benzopyran-2-oneHCID 19927678—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매IsopropanolHCID 3776—
생성물7-methoxy-3,4-dimethyl-6-[3-(4-phenyl-1-piperidinyl)propoxy]-2H-1-benzopyran-2-oneHCID 1992768164%

반응 단계

Method A (9 h at 60° C.); starting materials: 6-[3-(methanesulfonyloxy)propoxy]-7-methoxy-3,4-dimethyl-2H-1-benzopyran-2-one (example 75) and 4-phenylpiperidine; yield 64%; fusion point 152°-153° C. (from ethanol and isopropanol). Fumarate (×0.5 C4H4O4): method E; yield 92%; fusion point 209°-210° C. (from ethanol and methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428038
출처 데이터셋uspto-grants-1995_06
ORD IDord-27d533dd5f99403a86ddd4adb5d31e9f
출처 메모uspto-grants-1995_06