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4-Bromo-2-fluorotoluene → 5-Bromo-2-methylthioanisole

HRID 1406310
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HRID 1406310 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[C:4](F)[CH:3]=1.C(S)[CH2:11][S:12]([O-])(=O)=O.[Na+].C([O-])(O)=O.[Na+]>CN(C=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[C:4]([S:12][CH3:11])[CH:3]=1
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참가 물질

5

반응물 3

HCID 1710404-Bromo-2-fluorotolueneHCID 516892Sodium BicarbonateHCID 23662354Mesna

생성물 1

HCID 467393115-Bromo-2-methylthioanisole수율 70%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
90 °C

실험 절차

To a stirred solution of 4-bromo-2-fluoro-1-methyl-benzene (3 mL, 26.3 mmol) in DMF (15 mL) was added MeSNa (1.84 g, 26.3 mmol). After the addition, the reaction mixture was stirred at 90° C. overnight. TLC (petroleum) showed the reaction was complete. Then the mixture was poured into aq. NaHCO3 (10 mL), extracted with EtOAc (20 mL×2). The combined organic layers were washed with brine (50 mL×3), dried over sodium sulfate and concentrated in vacuum. The residue was purified by a silica gel column chromatography (petroleum) to give 4-Bromo-1-methyl-2-methylsulfanyl-benzene (4 g, 68%) as a yellow liquid.

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후처리

  1. additionAfter the addition
  2. extractionextracted with EtOAc (20 mL×2)
  3. washThe combined organic layers were washed with brine (50 mL×3)
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated in vacuum
  6. customThe residue was purified by a silica gel column chromatography (petroleum)

출처 및 근거

ORD 기록
ord-8675fac59cd04c5482098f0fc39064b5
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916593B2

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