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

HRID 1889017
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HRID 1889017 반응식
[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]
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참가 물질

4

반응물 2

HCID 24408BromineHCID 27742282,3-Difluorotoluene

생성물 1

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

시약·촉매·용매 1

HCID 23925Iron촉매

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-bf2c00c5912f487486b760ae5f4f21e3
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501946B2

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