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Anisole → HCID 13425547, 화합물

HRID 1249324
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HRID 1249324 반응식
F[B-](F)(F)F.[N+:6]([C:9]1[CH:10]=[C:11]([N+]#N)[CH:12]=[CH:13][CH:14]=1)([O-:8])=[O:7].C([O-])(=O)C.[K+].[C:22]1([O:28][CH3:29])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>>[CH3:29][O:28][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[C:11]1[CH:12]=[CH:13][CH:14]=[C:9]([N+:6]([O-:8])=[O:7])[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7519AnisoleHCID 517044Potassium AcetateHCID 11665863HCID 11665863, 화합물

생성물 1

HCID 13425547HCID 13425547, 화합물

실험 절차

Anisole (400 mL) and 3-nitrobenzenediazonium tetrafluoroborate (54.5 g, 0.23 mol) were placed in a 1-L flask and stirred mechanically. Potassium acetate (49.0 g, 0.5 mol) was added in one portion. The mixture turned red and warmed slightly. Stirring was continued 12 h., then the solution was filtered and the anisole evaporated in vacuo. Column chromatography of the residue (alumina, 0-10% ether/hexane, first yellow band) and recrystallization (95% EtOH) provided pure 2-methoxy-3'-nitrobiphenyl: 18 g (35%); mp 68°-69° C.

후처리

  1. temperaturewarmed slightly
  2. stirring
Stirring
  • filtrationthe solution was filtered
  • customthe anisole evaporated in vacuo
  • customColumn chromatography of the residue (alumina, 0-10% ether/hexane, first yellow band) and recrystallization (95% EtOH)
  • 출처 및 근거

    ORD 기록
    ord-d18e8faf045b4f39a44730e00eb674e4
    출처 데이터셋
    uspto-grants-1986_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04631119

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