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

HRID 1406310
ノート
印刷プレビュー

反応式

HRID 1406310 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 467393115-Bromo-2-methylthioanisole収率 70%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
90 °C

実験手順

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.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  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)

出典と根拠

ORDレコード
ord-8675fac59cd04c5482098f0fc39064b5
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08916593B2

反応ノート

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