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

3,4-Difluoroanisole → 1-Fluoro-4-methoxy-2-methylsulfanylbenzene

HRID 724256
노트
인쇄 미리보기

반응식

HRID 724256 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1F.[CH3:11][S-:12].[Na+]>CN(C)C=O.O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[S:12][CH3:11]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 5682503,4-DifluoroanisoleHCID 4378561Sodium methanethiolate2회

생성물 1

HCID 218772001-Fluoro-4-methoxy-2-methylsulfanylbenzene

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

반응 조건

온도
60 °C

실험 절차

1,2-Difluoro-4-methoxy-benzene (100 mg, 0.69 mmol) and sodium methanethiolate (148 mg, 2.08 mmol) were dissolved in N,N-dimethylformamide (2 mL) and the reaction mixture stirred at 60° C. for 18 hours. Additional sodium methanethiolate (99 mg, 139 mmol) was added and the reaction mixture heated to 100° C. for 18 hours. The reaction mixture was diluted with water and extracted with ether (x2). The ether extracts were washed with water (x2), dried over magnesium sulphate and concentrated in vacuo. The residue was taken up in pentane:ether 1:1 mixture (2 mL) and filtered through a plug of silica in a pipette, washing through with pentane:ether 1:1 mixture (5 mL). The solution was concentrated in vacuo to yield the title product as a colourless oil, 135 mg.

후처리

  1. temperaturethe reaction mixture heated to 100° C. for 18 hours
  2. extractionextracted with ether (x2)
  3. washThe ether extracts were washed with water (x2)
  4. dry with materialdried over magnesium sulphate
  5. concentrationconcentrated in vacuo
  6. filtrationfiltered through a plug of silica in a pipette
  7. washwashing through with pentane:ether 1:1 mixture (5 mL)
  8. concentrationThe solution was concentrated in vacuo

출처 및 근거

ORD 기록
ord-141050ea762b4c168e7b42b138ebb6c1
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07141586B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트