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Nitric Acid → N-[4-(1,1-dimethylethyl)-2-nitrophenyl]acetamide

HRID 1424239
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HRID 1424239 반응식
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12](=[O:14])[CH3:13])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].C(OC(=O)C)(=O)C.[N+:22]([O-])([OH:24])=[O:23]>C(O)(=O)C>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12](=[O:14])[CH3:13])=[C:7]([N+:22]([O-:24])=[O:23])[CH:6]=1)([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 7918Acetic AnhydrideHCID 1406724'-tert-Butylacetanilide

생성물 1

HCID 97069N-[4-(1,1-dimethylethyl)-2-nitrophenyl]acetamide수율 95.7%

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

실험 절차

A reactor was charged with acetic acid (8.7 L), followed by N-(4-tert-butylphenyl) acetamide (Preparation 110, 6.0 kg, 31.4 mol), The mixture was stirred for ten minutes, followed by the addition of acetic anhydride (6.47 kg, 63.4 mol) slowly at room temperature. The reaction was stirred for fifteen minutes. A solution of fuming nitric acid (3.56 kg, 56.5 mol) in acetic acid (2.1 L) was added slowly at 20-25° C., and stirred at that temperature for another 2 hours. The reaction mixture was added to ice water (42 L) at 10-15° C. and the mixture stirred for one hour. The resulting solids were collected by filtration, washed with water (17 L) and dried at 65-70° C. to provide 7.1 kg of the title compound.

후처리

  1. stirringThe reaction was stirred for fifteen minutes
  2. stirringstirred at that temperature for another 2 hours
  3. stirringthe mixture stirred for one hour
  4. filtrationThe resulting solids were collected by filtration
  5. washwashed with water (17 L)
  6. customdried at 65-70° C.

출처 및 근거

ORD 기록
ord-e785db7f392543eaaceeae56e2d7343e
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08927587B2

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