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

Phenanthridine → Phenanthridinesulfonic acid

HRID 1086452
노트
인쇄 미리보기

반응식

HRID 1086452 반응식
[CH:1]1[C:14]2[C:5](=[N:6][CH:7]=[C:8]3[C:13]=2[CH:12]=[CH:11][CH:10]=[CH:9]3)[CH:4]=[CH:3][CH:2]=1.Cl[S:16]([OH:19])(=[O:18])=[O:17]>>[C:1]1([S:16]([OH:19])(=[O:18])=[O:17])[C:14]2[C:5](=[N:6][CH:7]=[C:8]3[C:13]=2[CH:12]=[CH:11][CH:10]=[CH:9]3)[CH:4]=[CH:3][CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 9189PhenanthridineHCID 24638Chlorosulfonic acid

생성물 1

HCID 19826017Phenanthridinesulfonic acid수율 49.7%

반응 조건

온도
10 °C

실험 절차

Add phenanthridine (5 g, 28 mmol) in portions to chlorosulfonic acid (5.6 mL, 84 mmol) cooled to 10° C. over 20 minutes Heat the reaction mixture to reflux for 20 hours. Cool the now black reaction mixture to 0° C. and add cautiously to crushed ice (500 mL). Filter the solid and dry in vacuo to give the sulfonic acid (3.61 g) as an ivory colored solid consisting of a partially resolved 7:3 mixture of regioisomers. Rf=0.35 (major), 0.19 (minor (15:85 methanol:methylene chloride, 0.2% acetic acid buffer).

후처리

  1. temperatureHeat the reaction mixture
temperature
to reflux for 20 hours
  • temperatureCool the now black reaction mixture to 0° C.
  • additionadd cautiously
  • filtrationFilter the solid
  • customdry in vacuo
  • 출처 및 근거

    ORD 기록
    ord-55fbb317962e46f4968ca18f565c089a
    출처 데이터셋
    uspto-grants-1991_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05030631

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트