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

Potassium Permanganate → 1,2-Benzisothiazol-3(2H)-one, 5,6-dimethoxy-, 1,1-dioxide

HRID 259533
노트
인쇄 미리보기

반응식

HRID 259533 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]([O:10][CH3:11])=[CH:4][C:3]=1[S:12]([NH2:15])(=[O:14])=[O:13].[Mn]([O-])(=O)(=O)=[O:17].[K+]>[OH-].[Na+]>[CH3:9][O:8][C:6]1[C:5]([O:10][CH3:11])=[CH:4][C:3]2[S:12](=[O:14])(=[O:13])[NH:15][C:1](=[O:17])[C:2]=2[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 516875Potassium PermanganateHCID 352990334,5-Dimethoxy-2-methylbenzene-1-sulfonamide

생성물 1

HCID 470031361,2-Benzisothiazol-3(2H)-one, 5,6-dimethoxy-, 1,1-dioxide

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

16 gm (0.08 mol) of 2-methyl-4,5-dimethoxy-benzene sulfonamide were dissolved in 500 ml of an aqueous 5% sodium hydroxide solution, and the solution was heated at its boiling point for 2 hours after addition of 39.6 gm (0.25 mol) of potassium permanganate. After cooling, the reaction mixture was suction-filtered through celite, and the desired product was precipitated by addition of concentrated hydrochloric acid. Rf -value (benzene/acetone = 3/1): 0.2-0.4.

후처리

  1. temperaturethe solution was heated at its boiling point for 2 hours
  2. temperatureAfter cooling
  3. filtrationthe reaction mixture was suction-filtered through celite
  4. customthe desired product was precipitated by addition of concentrated hydrochloric acid

출처 및 근거

ORD 기록
ord-607d4c508e6e4f9fac3ed66c1e40bcb9
출처 데이터셋
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04038407

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트