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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22332생성일: 2026년 10월 25일

1-(3-Chloropropyl)-4-phenylpiperidine → 7-methoxy-4-(1-methylethyl)-6-[3-(4-phenyl-1-piperidinyl)propoxy]-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/22332

반응식

참여 물질

역할이름HCID투입량
반응물1-(3-Chloropropyl)-4-phenylpiperidineHCID 203689—
반응물FumarateHCID 5460307—
반응물HCID 19927654HCID 19927654—
용매AcetoneHCID 180—
용매tert-Butyl methyl etherHCID 15413—
생성물7-methoxy-4-(1-methylethyl)-6-[3-(4-phenyl-1-piperidinyl)propoxy]-2H-1-benzopyran-2-oneHCID 1992763885%

반응 단계

Method D (2.5 h at 85° C.); starting materials: 6-hydroxy-7-methoxy-4-(1-methylethyl)-2H-1-benzopyran-2-one (example 105) and 1-(3-chloropropyl)-4-phenyl-piperidine; yield 85%; fusion point 62°-65° C. (from TBME). Fumarate: method E; yield 65%; fusion point 155°-157° C. (from acetone, boiled out with TBME).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428038
출처 데이터셋uspto-grants-1995_06
ORD IDord-13dfe9d867b84ecfb63a521715149af8
출처 메모uspto-grants-1995_06