Sodium Carbonate → HCID 21319731, 화합물

HRID 262019노트

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HRID 262019 반응식
C[O-].[Na+].[Cl:4][C:5]1[CH:6]=[C:7]([NH:12][C:13](=[O:17])[N:14](C)C)[CH:8]=[CH:9][C:10]=1[OH:11].[Na].[CH3:19][C:20]([O:24][CH2:25]Cl)([CH3:23])[C:21]#[CH:22].C(=O)([O-])[O-].[Na+].[Na+]>CC(C)=O.O>[Cl:4][C:5]1[CH:6]=[C:7]([NH:12][C:13](=[O:17])[NH2:14])[CH:8]=[CH:9][C:10]=1[O:11][CH2:25][O:24][C:20]([CH3:23])([CH3:19])[C:21]#[CH:22]

참가 물질

8

실험 절차

Sodium methoxide (0.54 gram, 0.01 mole) is added to a methanolic solution of 3-(3-chloro-4-hydroxyphenyl)-1,1-dimethylurea (2.14 grams, 0.01 mole) and the mixture heated at reflux during 2 hours. The solvent is removed under reduced pressure and to the residual material dry benzene is added and evaporated off. This procedure is repeated until a dry white powder is obtained. The sodium salt is suspended in dry acetone (50 ml.) and chloromethyl 1,1-dimethyl-2-propynyl ether (1.45 grams, 0.011 mole) is added dropwise with stirring. After the initial exothermic reaction the reaction mixture is allowed to stir for a further 4.5 hours, then cold aqueous sodium carbonate solution (10% w/v, 100 ml.) followed by water (50 ml.) are added(1) and stirred. The resulting solid(2) is filtered off, water washed and air dried. Crystallization from benzene-hexane affords 2.2 grams, 70%; melting point 150° C. to 151° C. of Compound 1.

후처리

  1. temperaturethe mixture heated
  2. temperatureat reflux during 2 hours
  3. customThe solvent is removed under reduced pressure and to the residual material dry benzene
  4. additionis added
  5. customevaporated off
  6. customis obtained
  7. customAfter the initial exothermic reaction the reaction mixture
  8. stirringto stir for a further 4.5 hours
  9. stirringstirred
  10. filtrationThe resulting solid(2) is filtered off
  11. washwater washed
  12. customair dried
  13. customCrystallization from benzene-hexane
  14. customaffords 2.2 grams, 70%

출처 및 근거

ORD 기록
ord-7c66580e57a9456f812ad01eefb13dcc
출처 데이터셋
uspto-grants-1979_05
특허 번호
US04153448

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