Nitric Acid → N-(2-nitro-4-(oxetan-3-yl)phenyl)acetamide

HRID 511665

반응식

HRID 511665 반응식
[N+:1]([O-:4])(O)=[O:2].[O:5]1[CH2:8][CH:7]([C:9]2[CH:14]=[CH:13][C:12]([NH:15][C:16](=[O:18])[CH3:17])=[CH:11][CH:10]=2)[CH2:6]1.[N+]([O-])(O)=O.C(Cl)Cl.[NH4+].[OH-]>C(Cl)Cl>[N+:1]([C:11]1[CH:10]=[C:9]([CH:7]2[CH2:8][O:5][CH2:6]2)[CH:14]=[CH:13][C:12]=1[NH:15][C:16](=[O:18])[CH3:17])([O-:4])=[O:2]

참가 물질

6

반응물 4

HCID 944Nitric Acid2회HCID 14923Ammonium HydroxideHCID 20264123HNO3 dichloromethaneHCID 67776166N-(4-(Oxetan-3-YL)phenyl)acetamide

생성물 1

HCID 67776164N-(2-nitro-4-(oxetan-3-yl)phenyl)acetamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

The organic phase (upper phase) was isolated and the process was repeated with an additional 20 ml CH2Cl2. The organic extracts were combined, it was assumed the organic phase contained about 5 g (−80 mmol) of anhydrous HNO3. Using a 50 fold excess, this required about 25 ml of solution. The nitric acid solution was cooled in a ice bath. The N-(4-oxetan-3-ylphenyl)acetamide (21 0 mg, 0.70 mmol) was treated with 25 ml of the chilled HNO3/CH2Cl2 solution and was allowed to stir about 30 minutes. The reaction mixture was carefully poured into 45 ml 1 0% NH4OH solution and carefully shaken. The phases were separated and the aqueous phase was washed with 20 ml CH2Cl2. The combined organic phase was dried over Na2SO4, filtered and concentrated. The crude material was purified

후처리

  1. customThe organic phase (upper phase) was isolated
  2. stirringcarefully shaken
  3. customThe phases were separated
  4. washthe aqueous phase was washed with 20 ml CH2Cl2
  5. dry with materialThe combined organic phase was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude material was purified

출처 및 근거

ORD 기록
ord-e1917049c81346c38e02a6ec24682373
출처 데이터셋
uspto-grants-2015_08
특허 번호
US09096634B2

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