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Nitric Acid → Methyl 4-nitro-3-valerylaminobenzoate

HRID 653704
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HRID 653704 반응식
[C:1]([NH:7][C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][CH:17]=1)[C:11]([O:13][CH3:14])=[O:12])(=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5].[N+:18]([O-])([OH:20])=[O:19]>C(OC(=O)C)(=O)C.S(=O)(=O)(O)O>[N+:18]([C:17]1[CH:16]=[CH:15][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:9][C:8]=1[NH:7][C:1](=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5])([O-:20])=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 944Nitric AcidHCID 19171455Methyl 3-pentanamidobenzoate

생성물 1

HCID 19792184Methyl 4-nitro-3-valerylaminobenzoate수율 36%

시약·촉매·용매 2

HCID 1118Sulfuric Acid촉매HCID 7918Acetic Anhydride용매

실험 절차

To a solution of methyl 3-valerylaminobenzoate (2.3 g) in acetic anhydride (12 ml) was added dropwise fuming nitric acid (1.4 ml) while stirring under ice-cooling. To the mixture was added one drop of conc. sulfuric acid and the mixture was stirred for two hours. To the reaction mixture was added ice-water and it was extracted with ethyl acetate. The organic layer was washed with an aqueous solution of sodium bicarbonate and water and then dried. The solvent was evaporated to dryness, and the residue was purified by column chromatography on silica gel to afford a brown oil (1.0 g, 36%).

후처리

  1. temperaturecooling
  2. stirringthe mixture was stirred for two hours
  3. extractionwas extracted with ethyl acetate
  4. washThe organic layer was washed with an aqueous solution of sodium bicarbonate and water
  5. customdried
  6. customThe solvent was evaporated to dryness
  7. customthe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-a567ebbdcf7b48b3bb0ca57be5234510
출처 데이터셋
uspto-grants-1992_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05128356

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