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

HRID 1756817
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HRID 1756817 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 122755Glycine methyl ester hydrochlorideHCID 6453093Methylbutyrimidate

생성물 1

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

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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:

후처리

  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

출처 및 근거

ORD 기록
ord-9d1a34e626b142c68224aaabb99629bd
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05442075

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