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Potassium cyanate → 2,3-Dihydro-2-oxo-4,N,N-trimethyl-1H-imidazole-5-carboxamide

HRID 359704
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인쇄 미리보기

반응식

HRID 359704 반응식
[CH3:1][N:2]([CH3:11])[C:3](=[O:10])[C:4](=[N:8]O)[C:5](=O)[CH3:6].[H][H].[O-:14][C:15]#[N:16].[K+]>C(O)C.Cl.O>[O:14]=[C:15]1[NH:16][C:5]([CH3:6])=[C:4]([C:3]([N:2]([CH3:11])[CH3:1])=[O:10])[NH:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 11378442Potassium cyanateHCID 178418361HCID 178418361, 화합물HCID 178468379HCID 178468379, 화합물

생성물 1

HCID 128502882,3-Dihydro-2-oxo-4,N,N-trimethyl-1H-imidazole-5-carboxamide

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 702Ethanol용매

실험 절차

A solution of 15.8 g (0.1 mol) of N,N-dimethyl-2-(hydroxyimino)-3-oxobutanamide in 400 ml of ethanol and 100 ml of 2N hydrochloric acid over 2 g of catalyst (5% palladium on charcoal) is hydrogenated in a Paar shaker until 1 molar equivalent of hydrogen is taken up (3-5 hours). The catalyst is removed by filtration. A solution of 16.2 g (0.2 mol) of potassium cyanate in 80 ml of water is added, the solution is refluxed for 1 hour and concentrated until the product crystallizes. Recrystallization from 50% aqueous ethanol gives the title compound, m.p. 244°-246° C. (dec).

후처리

  1. custom(3-5 hours)
  2. customThe catalyst is removed by filtration
  3. temperaturethe solution is refluxed for 1 hour
  4. concentrationconcentrated until the product
  5. customcrystallizes
  6. customRecrystallization from 50% aqueous ethanol

출처 및 근거

ORD 기록
ord-ea34432a812544cba5f70cb2d8c99279
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05002961

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 962
Water
용매