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Dichloromethane → 4-Bromo-2-(bromomethyl)-1-iodobenzene

HRID 2220204
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HRID 2220204 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([I:10])=[C:6]([CH2:8]O)[CH:7]=1.P(Br)(Br)[Br:12].C(Cl)Cl.C([O-])(O)=O.[Na+]>CCl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([I:10])=[C:6]([CH2:8][Br:12])[CH:7]=1
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참가 물질

6

반응물 4

HCID 6344DichloromethaneHCID 24614Phosphorus tribromideHCID 516892Sodium Bicarbonate2회HCID 15339730(5-Bromo-2-iodophenyl)methanol

생성물 1

HCID 110033124-Bromo-2-(bromomethyl)-1-iodobenzene수율 52%

시약·촉매·용매 1

HCID 6327Methyl Chloride
용매

실험 절차

To a stirred mixture of (5-Bromo-2-iodo-phenyl)-m-ethanol (9.14 g, 29.2 mmol) in CH3Cl (150 mL) under argon was added 1M PBr3 in CH2Cl2 (35.0 mL, 35.0 mmol). The reaction mixture was stirred at room temperature for 20 min and then poured into a mixture of ice and saturated NaHCO3 solution (300 mL). The pH was adjusted to basic by addition of solid NaHCO3. This aqueous layer was extracted with EtOAc (1×600 mL, 2×400 mL). The combined EtOAc extracts were washed with brine (1×100 mL). The organic layer was dried (MgSO4), filtered and concentrated in vacuo to give 4-bromo-2-bromomethyl-1-iodo-benzene (5.69 g, 52%). 1H NMR (CDCl3): δ 7.68 (d, 1H, J=8.80 Hz), 7.59 (s, 1H), 7.18 (d, 1H, J=8.80 Hz), 4.51 (s, 2H). HPLC: Rt=3.87 min.

후처리

  1. extractionThis aqueous layer was extracted with EtOAc (1×600 mL, 2×400 mL)
  2. washThe combined EtOAc extracts were washed with brine (1×100 mL)
  3. dry with materialThe organic layer was dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-3c69d0280538416183f6572674fcf09f
출처 데이터셋
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07417040B2

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