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Bromine → 1-Bromo-3,4-difluoro-2-methylbenzene

HRID 1889017
ノート
印刷プレビュー

反応式

HRID 1889017 の反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[F:9].[Br:10]Br>[Fe]>[Br:10][C:5]1[CH:6]=[CH:7][C:2]([F:1])=[C:3]([F:9])[C:4]=1[CH3:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24408BromineHCID 27742282,3-Difluorotoluene

生成物 1

HCID 121376771-Bromo-3,4-difluoro-2-methylbenzene

試薬・触媒・溶媒 1

HCID 23925Iron触媒

実験手順

To 1,2-difluoro-3-methylbenzene (5 g, 39.0 mmol, commercially available from e.g. Sigma-Aldrich, Apollo or Fluorochem) containing iron (0.131 g, 2.342 mmol) was added bromine (2.011 ml, 39.0 mmol) dropwise maintaining a temperature of <30° C. with ice cooling. The mixture was stirred at room temperature overnight. The mixture was partitioned between water (50 mL) and diethyl ether (100 mL). The aqueous phase was extracted with diethyl ether (3×50 mL), combined organic extracts were washed with water (50 mL), 5% sodium thiosulfate solution (50 mL), water (50 mL), brine (50 mL), dried over anhydrous magnesium sulfate and concentrated in vacuo to afford product in 8.07 g. (Caution: by of product=68-70° C. @ 57 mBar).

後処理

  1. temperaturedropwise maintaining a temperature of <30° C. with ice cooling
  2. customThe mixture was partitioned between water (50 mL) and diethyl ether (100 mL)
  3. extractionThe aqueous phase was extracted with diethyl ether (3×50 mL)
  4. washwere washed with water (50 mL), 5% sodium thiosulfate solution (50 mL), water (50 mL), brine (50 mL)
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationconcentrated in vacuo
  7. customto afford product in 8.07 g
  8. custom(Caution: by of product=68-70° C. @ 57 mBar)

出典と根拠

ORDレコード
ord-bf2c00c5912f487486b760ae5f4f21e3
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08501946B2

反応ノート

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