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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344060생성일: 2026년 10월 26일

Pyridine → 2-[(5-Ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methoxycarbonyl]-1,1-diphenylhydrazine

https://huagongshe.com/reaction/344060

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물PhosgeneHCID 6371—
반응물Hydrazine, 1,1-diphenyl-, hydrochloride (1:1)HCID 10738—
반응물(5-Ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methanolHCID 53647005—
용매DichloromethaneHCID 6344—
생성물2-[(5-Ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methoxycarbonyl]-1,1-diphenylhydrazineHCID 70187314—

반응 단계

To a methylene chloride solution (1 ml) of phosgene dimer (0.027 ml) was added a methylene chloride solution (2 ml) of (5-ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methanol (0.12 g) and pyridine (0.1 ml) at -5° C., and the solution was stirred at room temperature for two hours. To the reaction mixture was added a solution of 1,1-diphenylhydrazine hydrochloride (0.10 g) and pyridine (0.05 ml) in methylene chloride (2 ml). The solution was stirred at room temperature for 3 hours, washed with 5% hydrochloric acid, water, and brine, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed (n-hexane-ethyl acetate) over silica gel to afford 2-[(5-ethoxycarbonylmethoxy-1,2,3,4-tetrahydro-1-naphthyl)methoxycarbonyl]-1,1-diphenyihydrazine (0.13 g) as colorless solids.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05863918
출처 데이터셋uspto-grants-1999_01
ORD IDord-5434fa9b16764b019f4f78cd116bcaef
출처 메모uspto-grants-1999_01