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

Dimethylformamide → Methyl 2-methyl-3-(methylthio)benzoate

HRID 906121
노트
인쇄 미리보기

반응식

HRID 906121 반응식
[SH:1][C:2]1[C:3]([CH3:11])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5](O)=[O:6].[C:12](=O)([O-])[O-].[Cs+].[Cs+].IC.CN(C)[CH:22]=[O:23]>C(OCC)(=O)C>[CH3:11][C:3]1[C:2]([S:1][CH3:12])=[CH:10][CH:9]=[CH:8][C:4]=1[C:5]([O:23][CH3:22])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 10796Cesium carbonateHCID 109318223-Mercapto-2-methylbenzoic acid

생성물 1

HCID 67404114Methyl 2-methyl-3-(methylthio)benzoate수율 58%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 3-mercapto-2-methylbenzoic acid (180 mg, 1.05 mmol), cesium carbonate (690 mg, 2.1 mmol) and iodomethane (132 L1, 2.10 mmol) in dimethylformamide (3 mL) was stirred at room temperature for 2 hours. The mixture was diluted with ethyl acetate then washed with 5% aqueous lithium chloride, 1N aqueous sodium hydroxide, and brine then dried over anhydrous sodium sulfate. Filtration and concentration afforded 138 mg, 0.62 mmol (58%) of methyl 2-methyl-3-(methylthio)benzoate. 1H NMR (400 MHz, CDCl3): 7.58 (d, 1H), 7.41 (d, 1H), 7.21-7.16 (m, 1H), 4.09 (s, 3H), 2.83 (s, 3H), 2.58 (s, 3H). MS (EI) for C10H12SO2: 197 (MH+).

후처리

  1. washthen washed with 5% aqueous lithium chloride, 1N aqueous sodium hydroxide, and brine
  2. dry with materialthen dried over anhydrous sodium sulfate
  3. filtrationFiltration and concentration

출처 및 근거

ORD 기록
ord-2e578a4f7d32431ba5db9e59042f0008
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08012956B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트