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Acetone → HCID 178457142、化合物

HRID 1866842
ノート
印刷プレビュー

反応式

HRID 1866842 の反応式
[C:1]1([C:7]2[N:8]=[C:9]([CH:12]([NH2:14])[CH3:13])[NH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:15][C:16]([CH3:18])=O>ClCCCl>[CH:16]([NH:14][CH:12]([C:9]1[NH:10][CH:11]=[C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[N:8]=1)[CH3:13])([CH3:18])[CH3:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 180AcetoneHCID 178463402HCID 178463402、化合物

生成物 1

HCID 178457142HCID 178457142、化合物

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

1-(4-Phenyl-1H-imidazol-2-yl)-ethylamine (0.20 g, 1.07 mmol) and acetone (0.062 g, 1.07 mmol) were mixed in 1,2-dichloroethane (4 mL), followed by the addition of NaBH(OAC)3 (0.34 g, 1.61 mmol). The resulting mixture was stirred at rt for 3 h. The reaction was quenched with saturated NaHCO3 solution. The mixture was extracted with EtOAc and the combined extracts were dried over Na2SO4. Filtration followed by evaporation to dryness under reduced pressure yielded crude isopropyl-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amine, which was used for the next reaction without further purification.

後処理

  1. customThe reaction was quenched with saturated NaHCO3 solution
  2. extractionThe mixture was extracted with EtOAc
  3. dry with materialthe combined extracts were dried over Na2SO4
  4. filtrationFiltration
  5. customfollowed by evaporation to dryness under reduced pressure

出典と根拠

ORDレコード
ord-cb7cad33cd764531877aa7dbbb71e20d
出典データセット
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07629488B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート