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

2-(2,5-Dimethoxybenzoyl)benzoic acid → 1,4-Dimethoxyanthraquinone

HRID 2397264
노트
인쇄 미리보기

반응식

HRID 2397264 반응식
[CH3:1][O:2][C:3]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][C:4]=1[C:5]([C:7]1[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=1[C:9]([OH:11])=O)=[O:6]>S(=O)(=O)(O)O>[CH3:21][O:20][C:17]1[C:16]2[C:9](=[O:11])[C:8]3[C:7](=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:5](=[O:6])[C:4]=2[C:3]([O:2][CH3:1])=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 3389962-(2,5-Dimethoxybenzoyl)benzoic acid

생성물 1

HCID 2660541,4-Dimethoxyanthraquinone

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

2-(2' ,5'-Dimethoxybenzoyl)-benzoic acid (I) (3 g, 0.01 mole) is added in portions to stirred concentrated sulfuric acid (20 ml). After addition the mixture is heated on steam bath with constant stirring for 20 minutes, cooled to room temperature and poured onto crushed ice (400 g) and extracted with chloroform (3 × 100 ml). The organic extract is washed with 2% aqueous sodium hydroxide solution (10 × 100 ml) and water (100 ml), then dried over anhydrous sodium sulfate and the solvent stripped off under reduced pressure to yield 1,4-dimethoxyanthraquinone (II), as a brownish yellow solid.

후처리

  1. additionAfter addition the mixture
  2. temperatureis heated on steam bath
  • additionpoured
  • extractionextracted with chloroform (3 × 100 ml)
  • extractionThe organic extract
  • washis washed with 2% aqueous sodium hydroxide solution (10 × 100 ml) and water (100 ml)
  • dry with materialdried over anhydrous sodium sulfate
  • 출처 및 근거

    ORD 기록
    ord-6416a724645c48e2a5e02de838028065
    출처 데이터셋
    uspto-grants-1977_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04021457

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트