홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

4-Aminophenol → 2-Chloro-3-(4-hydroxyanilino)-1,4-naphthoquinone

HRID 1895501
노트
인쇄 미리보기

반응식

HRID 1895501 반응식
Cl[C:2]1[C:3](=[O:14])[C:4]2[C:9]([C:10](=[O:13])[C:11]=1[Cl:12])=[CH:8][CH:7]=[CH:6][CH:5]=2.[CH:15]1[C:20]([NH2:21])=[CH:19][CH:18]=[C:17]([OH:22])[CH:16]=1>C(O)C>[Cl:12][C:11]1[C:10](=[O:13])[C:9]2[C:4]([C:3](=[O:14])[C:2]=1[NH:21][C:20]1[CH:15]=[CH:16][C:17]([OH:22])=[CH:18][CH:19]=1)=[CH:5][CH:6]=[CH:7][CH:8]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4034-AminophenolHCID 8342Dichlone

생성물 1

HCID 2605562-Chloro-3-(4-hydroxyanilino)-1,4-naphthoquinone

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

2,3-Dichloro-1,4-naphthoquinone (1.0 g, 4.4 mmol) was dissolved in 80 ml ethanol at 60° C., to which p-aminophenol (1.44 g, 13.2 mmol) in 20 ml ethanol was added. The reaction mixture was stirred at room temperature for 16 h. The precipitated product was filtered off and recrystallized from ethanol to afford pure purple crystals. Yield: 1.30 g (99%), Mp: 233° C.

후처리

  1. additionwas added
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
filtration
The precipitated product was filtered off
  • customrecrystallized from ethanol
  • customto afford pure purple crystals
  • 출처 및 근거

    ORD 기록
    ord-6127ee6e063b43549b10842add879073
    출처 데이터셋
    uspto-grants-2013_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08513437B2

    반응 노트

    불러오는 중…