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Sodium Hydroxide → 3,5-Dihydro-2-propyl-4H-imidazol-4-one

HRID 1756817
ノート
印刷プレビュー

反応式

HRID 1756817 の反応式
Cl.C[O:3][C:4](=O)[CH2:5][NH2:6].[OH-].[Na+].CO[C:12](=[NH:16])[CH2:13][CH2:14][CH3:15]>CO>[CH2:13]([C:12]1[NH:16][C:4](=[O:3])[CH2:5][N:6]=1)[CH2:14][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

5

反応物 3

HCID 14798Sodium HydroxideHCID 122755Glycine methyl ester hydrochlorideHCID 6453093Methylbutyrimidate

生成物 1

HCID 193917563,5-Dihydro-2-propyl-4H-imidazol-4-one

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

17.39 g (138 mmol) of glycine methyl ester hydrochloride was added to a solution of sodium hydroxide (5.56 g, 139 mmol) in methanol (55 ml) at 0° C. After 15 minutes, 14.50 g (content 96.3 percent, 138 mmol) of butanimidic acid methyl ester was instilled in the white suspension for 8 minutes. The mixture was stirred for 3 hours at room temperature and then concentrated by evaporation on a Rotavapor. The residue was mixed with CH2Cl2 (250 ml) and the resultant suspension was filtered. The filtrate was concentrated by evaporation on a Rotavapor, again mixed with CH2Cl2 (250 ml) and filtered again. After removal of the solvent, the title compound was obtained (15.13 g, content>95 percent according to 1H-NMR, 83 percent yield). Other data concerning the product was:

後処理

  1. concentrationconcentrated by evaporation on a Rotavapor
  2. additionThe residue was mixed with CH2Cl2 (250 ml)
  3. filtrationthe resultant suspension was filtered
  4. concentrationThe filtrate was concentrated by evaporation on a Rotavapor
  5. additionagain mixed with CH2Cl2 (250 ml)
  6. filtrationfiltered again
  7. customAfter removal of the solvent

出典と根拠

ORDレコード
ord-9d1a34e626b142c68224aaabb99629bd
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05442075

反応ノート

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