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Nitric Acid → 2-Nitro-5-(trifluoromethyl)phenol

HRID 567962
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HRID 567962 반응식
[N+:1]([O-:4])(O)=[O:2].[F:5][C:6]([F:15])([F:14])[C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([OH:13])[CH:8]=1>>[N+:1]([C:10]1[CH:11]=[CH:12][C:7]([C:6]([F:15])([F:14])[F:5])=[CH:8][C:9]=1[OH:13])([O-:4])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 944Nitric AcidHCID 73763-(Trifluoromethyl)phenol

생성물 1

HCID 140916902-Nitro-5-(trifluoromethyl)phenol수율 27%

실험 절차

2-Nitro-5-trifluoromethylphenol was prepared by adding concentrated HNO3 (6 mL) drop-wise to α,α,α-trifluoro-m-cresol (5 g, 30.8 mmol) at room temperature. After the addition was complete. the reaction was quenched with saturated ammonium acetate and extracted with EtOAc. The organic was separated, dried over sodium sulfate and filtered. Concentration of the solution in vacuo afforded an oil which was purified by column chromatography (gradient 100% hexane to 50% EtOAc/hexanes) to afford the titled compound as an oil(1.7 g, 27%). 1H NMR (CDCl3): 10.6 (s, 1H, OH), 8.26(d, 1H, J=7.8 Hz), 7.45(s, 1H, arom), 7.26(d, 1H, J=7.8 Hz).

후처리

  1. custom2-Nitro-5-trifluoromethylphenol was prepared
  2. additionAfter the addition
  3. customthe reaction was quenched with saturated ammonium acetate
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  • extractionextracted with EtOAc
  • customThe organic was separated
  • dry with materialdried over sodium sulfate
  • filtrationfiltered
  • customConcentration of the solution in vacuo afforded an oil which
  • customwas purified by column chromatography (gradient 100% hexane to 50% EtOAc/hexanes)
  • 출처 및 근거

    ORD 기록
    ord-9ad5b50795ba4db78e01af14024e0f20
    출처 데이터셋
    uspto-grants-2001_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06180675B2

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