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Nitric Acid → Methyl 5-nitro-2-(trifluoromethoxy)benzoate

HRID 967619
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HRID 967619 반응식
[N+:1]([O-:4])(O)=[O:2].[F:5][C:6]([F:19])([F:18])[O:7][C:8]1[CH:17]=[CH:16][CH:15]=[CH:14][C:9]=1[C:10]([O:12][CH3:13])=[O:11]>>[CH3:13][O:12][C:10](=[O:11])[C:9]1[CH:14]=[C:15]([N+:1]([O-:4])=[O:2])[CH:16]=[CH:17][C:8]=1[O:7][C:6]([F:5])([F:19])[F:18]
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참가 물질

3

반응물 2

HCID 944Nitric Acid2회HCID 2775550Methyl 2-(trifluoromethoxy)benzoate

생성물 1

HCID 46311174Methyl 5-nitro-2-(trifluoromethoxy)benzoate

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온도
60 °C

실험 절차

In a three-necked round bottom flask, equipped with a thermometer and a separatory funnel, HNO3 (5 mL fuming, 100%) was cooled in an ice bath. Methyl 2-(trifluoromethoxy)benzoate (5 g, 22.7 mmol) was slowly added to the cooled HNO3 within 0.5 hour while keeping the temperature below 15° C. The reacti0n was then stirred at 60° C. for 1 hour and 2 hours at room temperature. The mixture was added to ice water and an oil separated. The oily residue was added water (50 mL), neutralised with an aqueous solution of sodium hydrogen carbonate and then extracted with ethyl acetate (25 mL). The aqueous phase was extracted with ethyl acetate (15 mL) once more. The combined organic phases were washed with saturated sodium chloride (2×15 mL), dried (magnesium sulphate), and concentrated in vacuo to give 5.69 g of 5-nitro-2-trifluoromethoxybenzoic acid methyl ester.

후처리

  1. temperaturewas cooled in an ice bath
  2. customthe temperature below 15° C
  3. customan oil separated
  4. additionThe oily residue was added water (50 mL)
  5. extractionextracted with ethyl acetate (25 mL)
  6. extractionThe aqueous phase was extracted with ethyl acetate (15 mL) once more
  7. washThe combined organic phases were washed with saturated sodium chloride (2×15 mL)
  8. dry with materialdried (magnesium sulphate)
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-6959f3b76099402e9e47d708039186f5
출처 데이터셋
uspto-grants-2005_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06953812B2

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