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

Hydrogen Bromide → N-benzyl-5,6-dihydroxy-N-methylisoindolinium bromide

HRID 1032482
노트
인쇄 미리보기

반응식

HRID 1032482 반응식
[I-].[CH2:2]([N+:9]1([CH3:22])[CH2:17][C:16]2[C:11](=[CH:12][C:13]([O:20]C)=[C:14]([O:18]C)[CH:15]=2)[CH2:10]1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[BrH:23]>>[Br-:23].[CH2:2]([N+:9]1([CH3:22])[CH2:10][C:11]2[C:16](=[CH:15][C:14]([OH:18])=[C:13]([OH:20])[CH:12]=2)[CH2:17]1)[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 260Hydrogen BromideHCID 14993733HCID 14993733, 화합물

생성물 1

HCID 14993734N-benzyl-5,6-dihydroxy-N-methylisoindolinium bromide

반응 조건

온도
120 °C

실험 절차

To 10 g (24.3 mmol) of N-benzyl-5,6-dimethoxy-N-methylisoindolinium iodide, 50 ml of 48% hydrobromic acid was added, and the mixture was heated at reflux for 3 hours at an external temperature of 120° C. The reaction solution was evaporated to dryness under reduced pressure, and the crystal residue was washed with 20 ml of acetone to obtain 6.90 g of the above identified compound. The filtrate was left to stand overnight, to obtain 190 mg of the secondary crystals. The total yield was 7.09 g. The melting point, the infrared absorption spectrum and the 1H-NMR spectrum of this product agreed to those of Example 2.

후처리

  • temperaturethe mixture was heated
  • customThe reaction solution was evaporated to dryness under reduced pressure
  • washthe crystal residue was washed with 20 ml of acetone
  • customto obtain 6.90 g of the
  • waitThe filtrate was left
  • 출처 및 근거

    ORD 기록
    ord-0b6469ff780e4eb2af4f2afb16b8129d
    출처 데이터셋
    uspto-grants-1990_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04958029

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트