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

Sodium Hydroxide → 1-Methylsulfinyl-1-methylthio-2-(m-benzoylphenyl)ethylene

HRID 614251
노트
인쇄 미리보기

반응식

HRID 614251 반응식
[C:1]([C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH:12]=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:17][S:18][CH2:19][S:20]([CH3:22])=[O:21].[OH-].[Na+]>O>[CH3:22][S:20]([C:19]([S:18][CH3:17])=[CH:12][C:11]1[CH:14]=[CH:15][CH:16]=[C:9]([C:1](=[O:8])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH:10]=1)=[O:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 99129Methyl (methylsulfinyl)methyl sulfideHCID 130201683-Benzoylbenzaldehyde

생성물 1

HCID 541901371-Methylsulfinyl-1-methylthio-2-(m-benzoylphenyl)ethylene

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
95 °C

실험 절차

m-Benzoylbenzaldehyde (902 mg) was added to 1 ml of FAMSO, and 60 mg of sodium hydroxide was added. The mixture was stirred at 95° C. for 70 minutes in an atmosphere of argon. Water (20 ml) was added, and the reaction mixture was extracted with methylene chloride. The organic layer was dried over anhydrous sodium sulfate, concentrated under reduced pressure, and chromatographed on a silica gel column using methylene chloride as an eluant to afford 1.035 g of 1-methylsulfinyl-1-methylthio-2-(m-benzoylphenyl)ethylene.

후처리

  1. additionwas added
  2. extractionthe reaction mixture was extracted with methylene chloride
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customchromatographed on a silica gel column

출처 및 근거

ORD 기록
ord-cbd5e9837fc14945a2503c53069e1c2a
출처 데이터셋
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04144248

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트