Hydrochloric Acid → HCID 12876121, 화합물

HRID 847813노트

반응식

HRID 847813 반응식
ClCCl.[CH3:4][N:5]([CH2:10][CH2:11][CH3:12])[C:6]([NH:8][CH3:9])=[O:7].[C:13]1([N:19]=[C:20]=[O:21])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.Cl>C(Cl)(Cl)Cl>[CH3:4][N:5]([CH2:10][CH2:11][CH3:12])[C:6]([N:8]([CH3:9])[C:20]([NH:19][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:21])=[O:7]

참가 물질

6

실험 절차

Into 300 ml of anhydrous dichloromethane, 13.0 g (0.1 mol) of 1,3-dimethyl-1-propylurea and 12.0 g (0.1 mol) of phenylisocyanate were added and dissolved. The mixture was ice-cooled under stirring and 26.0 g (0.1 mol) of stannic chloride was added drop-wise. The reaction was then continued at a room temperature for 15 hours and the precipitate formed was separated by filtration. The precipitate thus obtained was added into a mixture of 60 ml of 20% hydrochloric acid/120 ml of chloroform and the stirring was continued until the mixture became transparent. Then the chloroform layer was separated and was washed with water and the chloroform layer was dried with anhydrous sodium sulfate. The chloroform was removed by distillation under reduced pressure and the residue thus obtained was recrystallized from ligroin to obtain 18.6 g (yield: 75%) of 1,3-dimethyl-1-propyl-5-phenylbiuret having a melting point of 63° to 64° C.

후처리

  1. dissolutiondissolved
  2. temperaturecooled
  3. customthe precipitate formed
  4. customwas separated by filtration
  5. customThe precipitate thus obtained
  6. customThen the chloroform layer was separated
  7. washwas washed with water
  8. dry with materialthe chloroform layer was dried with anhydrous sodium sulfate
  9. customThe chloroform was removed by distillation under reduced pressure
  10. customthe residue thus obtained
  11. customwas recrystallized from ligroin

출처 및 근거

ORD 기록
ord-fe053f5bdafe40a7b4807a79593869d1
출처 데이터셋
uspto-grants-1981_10
특허 번호
US04293713

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