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Imidazole → N-1H-Inden-3-ylacetamide

HRID 1582778
ノート
印刷プレビュー

反応式

HRID 1582778 の反応式
[C:1]1(=[N:10]O)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.N1C=CN=C1.[C:17](OC(=O)C)(=[O:19])[CH3:18].C(=O)([O-])[O-].[Na+].[Na+]>C(#N)C.C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C.[Ti+3]>[C:17]([NH:10][C:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH:2]=1)(=[O:19])[CH3:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 795ImidazoleHCID 7918Acetic Anhydride2 回HCID 10340Sodium CarbonateHCID 3023232,3-Dihydro-1H-inden-1-one oxime

生成物 1

HCID 10130185N-1H-Inden-3-ylacetamide収率 61.3%

試薬・触媒・溶媒 2

HCID 14117218HCID 14117218、化合物
触媒
HCID 6342Acetonitrile溶媒

実験手順

1-Indanone oxime (2.33 g, 0.016 moles) and imidazole (78 mg) in acetonitrile (45 ml) cooled in ice, were treated with acetic anhydride (11 ml, 0.12 moles) and the mixture thus stirred for one hour. Titanium triacetate (17 g) was added, followed by more acetic anhydride (11 ml, 0.12 moles). The mixture was brought to reflux under nitrogen. After 2 hours the mixture was allowed to cool, poured into 1M sodium carbonate (250 ml) and stirred for 15 minutes. Three-fold extraction with ethyl acetate, drying (MgSO4) and evaporation left a brown oil which was reevaporated with toluene. The brown residue was subjected to flash chromatography on silica gel with ethyl acetate/hexane 1:2 v/v. The major component was obtained as a white solid (1.7 g) from the appropriate fractions and was recrystallized from ethyl acetate/hexane to give the title compound, mp 137-138° C. (1.45 g, 52.9%).

後処理

  1. temperatureto reflux under nitrogen
  2. waitAfter 2 hours the mixture was allowed
  3. temperatureto cool
  4. stirringstirred for 15 minutes
  5. extractionThree-fold extraction with ethyl acetate
  6. customdrying
  7. custom(MgSO4) and evaporation
  8. waitleft a brown oil which
  9. customwas reevaporated with toluene

出典と根拠

ORDレコード
ord-d94c586946924f86bae69c005a79c13c
出典データセット
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06737547B1

反応ノート

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