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Imidazole → 1-[4-(4-t-Butylphenyl)butan-4-onyl]imidazole

HRID 463280
ノート
印刷プレビュー

反応式

HRID 463280 の反応式
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[C:6]([C:10]1[CH:15]=[CH:14][C:13]([C:16](=[O:21])[CH2:17][CH2:18][CH2:19]Cl)=[CH:12][CH:11]=1)([CH3:9])([CH3:8])[CH3:7]>CN(C)C=O>[C:6]([C:10]1[CH:11]=[CH:12][C:13]([C:16](=[O:21])[CH2:17][CH2:18][CH2:19][N:1]2[CH:5]=[CH:4][N:3]=[CH:2]2)=[CH:14][CH:15]=1)([CH3:9])([CH3:8])[CH3:7]
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 795ImidazoleHCID 27236944'-tert-Butyl-4-chlorobutyrophenone

生成物 1

HCID 202824961-[4-(4-t-Butylphenyl)butan-4-onyl]imidazole収率 80.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a 0° C. slurry of 8.24 g of imidazole in 15 ml. dry dimethylformamide was added 5.79 g of p-t-butyl-gamma-chlorobutyrophenone and the mixture was stirred overnight at room temperature, then for one day at 60° C. The above solution was poured into 400 ml. of water and extracted three times with ethyl acetate. The combined extracts were washed with water, dried over magnesium sulfate and the solvent evaporated to afford 5.25 g of 1-[4-(4-t-butylphenyl)butan-4-onyl]imidazole as a golden oil.

後処理

  1. customTo a 0° C.
  2. waitfor one day at 60° C
  3. additionThe above solution was poured into 400 ml
  4. extractionof water and extracted three times with ethyl acetate
  5. washThe combined extracts were washed with water
  6. dry with materialdried over magnesium sulfate
  7. customthe solvent evaporated

出典と根拠

ORDレコード
ord-5474642cacfe4a3b81f6d870e9488a59
出典データセット
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04518607

反応ノート

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