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Acetic Acid → 4,5-Dimethyl-1-(3-nitrophenyl)imidazole

HRID 1835474
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HRID 1835474 반응식
[CH3:1][CH:2]([N:6]([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([N+:15]([O-:17])=[O:16])[CH:10]=1)[CH:7]=O)[C:3](=O)[CH3:4].C([O-])(=O)C.[NH4+:22].C(O)(=O)C.[OH-].[Na+]>C1(C)C(C)=CC=CC=1.C(OCC)(=O)C>[CH3:4][C:3]1[N:22]=[CH:7][N:6]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([N+:15]([O-:17])=[O:16])[CH:10]=2)[C:2]=1[CH3:1]
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참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 517165Ammonium AcetateHCID 23503659N-(1-methyl-2-oxo-propyl)-N-(3-nitrophenyl)formamide

생성물 1

HCID 235036474,5-Dimethyl-1-(3-nitrophenyl)imidazole수율 73.4%

시약·촉매·용매 2

HCID 7237O-Xylene
용매
HCID 8857Ethyl Acetate용매

실험 절차

A suspension of N-(1-methyl-2-oxo-propyl)-N-(3-nitrophenyl)formamide (1.17 g), ammonium acetate (3.82 g) and acetic acid (1 ml) in xylene (20 ml) was refluxed for 2 hours. After adding ethyl acetate and an aqueous solution of sodium hydroxide (1N, 100 ml), the mixture was stirred for 10 minutes. The separated aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified with a silica gel column chromatography eluting with 1-3% unethanol/dichloromethane to give 4,5-dimethyl-1-(3-nitrophenyl)imidazole (0.79 g, 73.1%).

후처리

  1. temperaturewas refluxed for 2 hours
  2. extractionThe separated aqueous layer was extracted with ethyl acetate
  3. washThe combined organic layers were washed with water and brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated under reduced pressure
  6. customThe residue was purified with a silica gel column chromatography
  7. washeluting with 1-3% unethanol/dichloromethane

출처 및 근거

ORD 기록
ord-7850bd0863fc47e4ba0fa9ec4933ede5
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06770667B1

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