Dimethylformamide → 5-Bromo-1,3-dimethyl-2-(methylsulfanyl)benzene

HRID 748965

반응식

HRID 748965 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH3:10])[C:5](F)=[C:6]([CH3:8])[CH:7]=1.CN(C)C=O.[CH3:16][S-:17].[Na+]>O.C(OCC)C>[Br:1][C:2]1[CH:3]=[C:4]([CH3:10])[C:5]([S:17][CH3:16])=[C:6]([CH3:8])[CH:7]=1

참가 물질

6

반응물 3

HCID 6228DimethylformamideHCID 27362985-Bromo-2-fluoro-1,3-dimethylbenzeneHCID 4378561Sodium methanethiolate

생성물 1

HCID 685195015-Bromo-1,3-dimethyl-2-(methylsulfanyl)benzene수율 14.2%

시약·촉매·용매 2

HCID 962Water용매HCID 3283Diethyl Ether용매

반응 조건

온도
50 °C

실험 절차

Add 5-bromo-2-fluoro-1,3-dimethyl-benzene (3.5 g, 17.2 mmol) to dimethylformamide (DMF, 30 mL) at ambient temperature followed by sodium thiomethoxide (1.32 g, 17.9 mmol). Heat at 50° C. for 8 hours and dilute with water (10 mL) and diethyl ether (100 mL). Separate the layers, wash the organics with brine, and dry with magnesium sulfate before concentrating to a residue. Chromatograph the residue on a SiO2 column eluting with diethyl ether (20%) in hexane to give 566 mg (14%) of 5-bromo-1,3-dimethyl-2-methylsulfanyl-benzene.

후처리

  1. customSeparate the layers
  2. washwash the organics with brine
  3. dry with materialdry with magnesium sulfate
  4. concentrationbefore concentrating to a residue
  5. washChromatograph the residue on a SiO2 column eluting with diethyl ether (20%) in hexane

출처 및 근거

ORD 기록
ord-0bea027b62d54eb7954dc8da2e4cd887
출처 데이터셋
uspto-grants-2008_07
특허 번호
US07399867B2

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