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Trifluoroacetic anhydride → 4-Methoxy-3-nitrobenzaldehyde

HRID 470609
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인쇄 미리보기

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HRID 470609 반응식
[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[CH:5][CH:4]=1.[N+:11]([O-])([O-:13])=[O:12].[NH4+].FC(F)(F)C(OC(=O)C(F)(F)F)=O>>[CH3:1][O:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[CH:5][C:4]=1[N+:11]([O-:13])=[O:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 9845Trifluoroacetic anhydrideHCID 22985Ammonium nitrateHCID 312444-Methoxybenzaldehyde

생성물 1

HCID 7006084-Methoxy-3-nitrobenzaldehyde

반응 조건

온도
0 °C

실험 절차

4-Methoxy-benzaldehyde (1 g, 7.34 mmol) was added to a mixture of ammonium nitrate (0.58 g, 7.34 mmol) and trifluoroacetic anhydride (3.56 mL, 25.69 mmol), which was cooled to 0° C. The reaction mixture was stirred at 0° C. for 15 min and then allowed to stir at room temperature for about 7 h. Ice was added and stirred for 30 min. The solid obtained was filtered, washed with cold water (3×5 mL) and dried.

후처리

  1. stirringto stir at room temperature for about 7 h
  2. additionIce was added
  3. stirringstirred for 30 min
  4. customThe solid obtained
  5. filtrationwas filtered
  6. washwashed with cold water (3×5 mL)
  7. customdried

출처 및 근거

ORD 기록
ord-6067fa5cc097451e81cbc27fe97363dc
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08629277B2

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