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Nitric Acid → N,N'-[1-(4-Nitrophenyl)ethane-1,2-diyl]diacetamide

HRID 441935
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HRID 441935 반응식
[C:1]([NH:4][CH:5]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH2:6][NH:7][C:8](=[O:10])[CH3:9])(=[O:3])[CH3:2].C([O-])(O)=O.[Na+].[N+:22]([O-])([OH:24])=[O:23]>>[C:1]([NH:4][CH:5]([C:11]1[CH:12]=[CH:13][C:14]([N+:22]([O-:24])=[O:23])=[CH:15][CH:16]=1)[CH2:6][NH:7][C:8](=[O:10])[CH3:9])(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 944Nitric AcidHCID 516892Sodium BicarbonateHCID 12698223N,N'-(1-Phenylethane-1,2-diyl)diacetamide

생성물 1

HCID 13050187N,N'-[1-(4-Nitrophenyl)ethane-1,2-diyl]diacetamide수율 61%

실험 절차

3 g, 0.014 mol of N,N'-Diacetyl-1-phenylethylenediamine was added slowly to 10 ml of 90% HNO3 at -40°. After stirring 5 hr at -40°, the solution was poured over ice and neutralized with NaHCO3. The product was extracted into ethyl acetate, and that was dried with MgSO4 and then evaporated to dryness under reduced pressure. The product was recrystallized from acetone/hexane, yielding 2.2 g (61%) of N,N'-Diacetyl-1-(p-nitrophenyl)-ethylenediamine mp 178°-180°. Anal. (C12H15N3O4) C, H, N were within 0.4% of theoretical.

후처리

  1. extractionThe product was extracted into ethyl acetate
  2. dry with materialthat was dried with MgSO4
  3. customevaporated to dryness under reduced pressure
  4. customThe product was recrystallized from acetone/hexane

출처 및 근거

ORD 기록
ord-84079c942a4e4614a42603079a367309
출처 데이터셋
uspto-grants-1977_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04043998

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