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Acetone → HCID 178440097、化合物

HRID 53033
ノート
印刷プレビュー

反応式

HRID 53033 の反応式
[BH4-].[Na+].[C:3]([C:6]1[N:7]=[C:8]([CH2:16][CH2:17][CH3:18])[NH:9][C:10]=1[C:11]([O:13][CH2:14][CH3:15])=[O:12])(=[O:5])[CH3:4].CC(C)=O>C(O)C>[OH:5][CH:3]([C:6]1[N:7]=[C:8]([CH2:16][CH2:17][CH3:18])[NH:9][C:10]=1[C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 180AcetoneHCID 4311764Sodium borohydrideHCID 10513320ethyl 4-acetyl-2-propyl-1H-imidazole-5-carboxylate

生成物 1

HCID 178440097HCID 178440097、化合物収率 87.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

125 mg of sodium borohydride were added to a solution of 1.50 g of ethyl 4-acetyl-2-propylimidazole-5-carboxylate [prepared as described in step (ii) above] in 15 ml of ethanol, and the resulting mixture was stirred at room temperature for 30 minutes. 2 ml of acetone were added, and the mixture was stirred for a further 10 minutes. The reaction mixture was then concentrated by evaporation under reduced pressure, and the concentrate was dissolved in methanol. The solution was again concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel, using 1:20 and 1:10 by volume mixtures of methylene chloride and methanol as the eluent, to give 1.32 g of the title compound as crystals, melting at 151°-153° C.

後処理

  1. stirringthe mixture was stirred for a further 10 minutes
  2. concentrationThe reaction mixture was then concentrated by evaporation under reduced pressure
  3. dissolutionthe concentrate was dissolved in methanol
  4. concentrationThe solution was again concentrated by evaporation under reduced pressure
  5. customthe residue was purified by column chromatography through silica gel

出典と根拠

ORDレコード
ord-f722cfd71cc94e1aa106548e3474c1f3
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05616599

反応ノート

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