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

Water → 1-Methyl-2-nitro-4-(phenylsulfonyl)benzene

HRID 2390196
노트
인쇄 미리보기

반응식

HRID 2390196 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:4][C:3]=1[N+:15]([O-:17])=[O:16].[OH:18]OS([O-])=O.[K+].[OH2:24]>CO>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)(=[O:18])=[O:24])=[CH:4][C:3]=1[N+:15]([O-:17])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962Water2회HCID 23707502Potassium hydroxy sulfiteHCID 565939751-Methyl-2-nitro-4-(phenylthio)benzene2회

생성물 1

HCID 565939761-Methyl-2-nitro-4-(phenylsulfonyl)benzene수율 82%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 1-methyl-2-nitro-4-(phenylthio)benzene (Intermediate 111; 745 mg; 3.04 mmol) in MeOH (11 ml) and water (11 ml) was treated with Oxone® (5.60 g; 9.11 mmol) and the reaction mixture was stirred at RT for 6 hours. Water was added and the reaction mixture was extracted 2 times with DCM. The combined organic extracts were dried over MgSO4, filtered and concentrated to dryness affording the title compound as a beige solid (690 mg, 82%).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. extractionthe reaction mixture was extracted 2 times with DCM
  2. dry with materialThe combined organic extracts were dried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-4c7a111b1edd414a89f9f07d56f679e5
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08273769B2

반응 노트

불러오는 중…