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Boron tribromide → 4-Bromo-3-nitrophenol

HRID 431389
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HRID 431389 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8]C)=[CH:4][C:3]=1[N+:10]([O-:12])=[O:11].B(Br)(Br)Br>ClCCl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[N+:10]([O-:12])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25134Boron tribromide2회HCID 792884-Bromo-3-nitroanisole

생성물 1

HCID 158178674-Bromo-3-nitrophenol수율 68.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of 1-bromo-4-methoxy-2-nitrobenzene (2.32 g, 10 mmol) in 75 mL of dichloromethane at 0° C. was added BBr3 solution (1 M in DCM, 12 mL, 12 mmol) dropwise. The solution was allowed to warm to room temperature and stirred for 16 h. GC/MS showed starting material still left so another 12 mL of BBr3 solution was added and the reaction mixture refluxed for 4 h. The reaction mixture was cooled in ice and quenched with water. After washing successively with saturated NaHCO3(aq) and brine, the organic layer was dried over MgSO4, filtered and evaporated. The resulting yellow solid was flash chromatographed (25% EtOAc/hexane) to give 1.5 g of product in (69%) yield as a pale yellow solid: MS (EI) m/z 218 (M+).

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후처리

  1. additionwas added
  2. temperaturethe reaction mixture refluxed for 4 h
  3. temperatureThe reaction mixture was cooled in ice
  4. customquenched with water
  5. washAfter washing successively with saturated NaHCO3(aq) and brine
  6. dry with materialthe organic layer was dried over MgSO4
  7. filtrationfiltered
  8. customevaporated
  9. customchromatographed (25% EtOAc/hexane)

출처 및 근거

ORD 기록
ord-104232f3e11146ffb929231e07ad212a
출처 데이터셋
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06656971B2

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