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

Maleic Anhydride → 1H-Pyrrole-2,5-dione, 1-(2,4,6-tribromophenyl)-

HRID 247164
노트
인쇄 미리보기

반응식

HRID 247164 반응식
[Br:1][C:2]1[CH:8]=[C:7]([Br:9])[CH:6]=[C:5]([Br:10])[C:3]=1[NH2:4].[C:11]1(=O)[O:16][C:14](=[O:15])[CH:13]=[CH:12]1.[Sn](Cl)Cl>>[Br:1][C:2]1[CH:8]=[C:7]([Br:9])[CH:6]=[C:5]([Br:10])[C:3]=1[N:4]1[C:14](=[O:15])[CH:13]=[CH:12][C:11]1=[O:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7923Maleic AnhydrideHCID 89862,4,6-TribromoanilineHCID 24479Stannous Chloride

생성물 1

HCID 30171561H-Pyrrole-2,5-dione, 1-(2,4,6-tribromophenyl)-

반응 조건

온도
142 °C

실험 절차

A mixture of 2,4,6-tribromoaniline (1.20g, 3.64 mmol), maleic anhydride (0.83g, 8.5 mmol) and tin(II) chloride (0.064g, 0.34 mmol) is heated to 142° C. with mixing and held at this temperature for 1.9 hours. The reaction mixture is cooled, extracted with xylene, filtered and the resulting filtrate water washed. Solvent removal yielded N-(2,4,6-tribromophenyl)maleimide. Analysis by High Pressure Liquid Chromatography (HPLC) showed conversion of 2,4,6-tribromoaniline to be 99.9% and selectivity to N-(2,4,6-tribromophenyl)maleimide based on reacted 2,4,6-tribromoaniline of 75.0%.

후처리

  1. additionwith mixing
  2. temperatureThe reaction mixture is cooled
  3. extractionextracted with xylene
  4. filtrationfiltered
  5. washthe resulting filtrate water washed
  6. customSolvent removal

출처 및 근거

ORD 기록
ord-18dd8ed719df4f0388642cdc678801c0
출처 데이터셋
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04705866

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트