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

Sodium Hydroxide → 2-Methylanthraquinone

HRID 1728945
노트
인쇄 미리보기

반응식

HRID 1728945 반응식
[OH-].[Na+].S([O-])(O)=O.[Na+].[CH3:8][C:9]1[C:10](=[O:20])[C:11]2[C:16]([C:17](=[O:19])[CH:18]=1)=[CH:15][CH:14]=[CH:13][CH:12]=2>>[CH3:10][C:9]1[CH:18]=[CH:8][C:9]2[C:10](=[O:20])[C:11]3[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=3)[C:17](=[O:19])[C:18]=2[CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 14798Sodium HydroxideHCID 236949362-Methyl-1,4-naphthoquinone sodium hydrogensulfite

생성물 1

HCID 67732-Methylanthraquinone

실험 절차

A 0.5N aqueous sodium hydroxide solution was added to the oil phase obtained in Example 14, and, after 30 minutes stirring, air was blown thereinto at 70° C. for 2 hours. Then, the oil phase and the aqueous phase containing the precipitate were separated, and the aqueous phase was dried under reduced pressure to obtain 5.5 kg of 2-methylanthraquinone.

후처리

  1. waitat 70° C. for 2 hours
  2. additionThen, the oil phase and the aqueous phase containing the precipitate
  3. customwere separated
  4. customthe aqueous phase was dried under reduced pressure

출처 및 근거

ORD 기록
ord-8413aed7ab6d412189a9f71f8dc2eb86
출처 데이터셋
uspto-grants-1994_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05329026

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트