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Methanol → 2-Methoxy-2'-nitro-4,4'-dibromobiphenyl

HRID 79852
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HRID 79852 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([Br:14])=[CH:10][C:9]=2[N+:15]([O-:17])=[O:16])=[C:4]([N+]([O-])=O)[CH:3]=1.[CH3:21][O-:22].[Na+].CO>CN(C=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([Br:14])=[CH:10][C:9]=2[N+:15]([O-:17])=[O:16])=[C:4]([O:22][CH3:21])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 100466484,4'-Dibromo-2,2'-dinitro-1,1'-biphenylHCID 10942334Sodium Methoxide

생성물 1

HCID 99774712-Methoxy-2'-nitro-4,4'-dibromobiphenyl

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
25 °C

실험 절차

To the solution of 4,4′-dibromo-2,2′-dinitro-biphenyl (6.58 g, 16.5 mmol) in DMF (50 ml) at 0° C. was added a solution of sodium methoxide in Methanol (4.4 M, 4.5 ml, 19.8 mmol). The mixture was stirred at 25° C. for 12 hours and was poured into ice-water (140 ml). The mixture was extracted with EtOAc (2×). The combined organic phase was washed with water and brine and dried with Na2SO4. Concentration under reduced pressure gave pale solid. The re-crystallization from CH3CN/MeOH gave 4,4′-dibromo-2-methoxy-2′-nitro-biphenyl as a white solid (3.76 g).

후처리

  1. extractionThe mixture was extracted with EtOAc (2×)
  2. washThe combined organic phase was washed with water and brine
  3. dry with materialdried with Na2SO4
  4. concentrationConcentration under reduced pressure
  5. customgave pale solid
  6. customThe re-crystallization from CH3CN/MeOH

출처 및 근거

ORD 기록
ord-a82ef3c06d9e4a16872ba8ff2dba8161
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08841278B2

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