Ammonia → (4'-Dimethylamino phenyl]-3-ureido benzoquinoneimine

HRID 1413039

反応式

HRID 1413039 の反応式
[NH:1]([C:5]1[CH:6]=[C:7]([OH:11])[CH:8]=[CH:9][CH:10]=1)[C:2]([NH2:4])=[O:3].[NH3:12].C1(N)C(F)=C(F)C(F)=C(N)C=1F.Cl.Cl.[CH3:27][N:28]([CH3:36])[C:29]1[CH:34]=[CH:33][C:32](N)=[CH:31][CH:30]=1.S(OOS([O-])(=O)=O)([O-])(=O)=O.[NH4+].[NH4+].[OH2:49]>C(O)(C)C>[CH3:27][N:28]([CH3:36])[C:29]1[CH:34]=[CH:33][C:32]([C:9]2[C:10](=[O:49])[CH:5]([NH:1][C:2]([NH2:4])=[O:3])[C:6](=[NH:12])[C:7](=[O:11])[CH:8]=2)=[CH:31][CH:30]=1

参加物

8

反応条件

温度
0 °C

実験手順

0.03 mole (4.56 g) of 3-ureido phenol is dissolved in 100 cc of isopropyl alcohol to which have been added 100 cc of ammonia at 22° Be. 350 g of crushed ice are then added to this solution. The resulting reaction mixture is maintained at about 0° C., and there are introduced simultaneously, with good agitation and with the aid of a double funnel, 0.03 mole (6.27 g) of the dihydrochloride of N,N-dimethyl paraphenylenediamine in 50 cc of water and 0.060 mole (13.7 g) of ammonium persulfate in 50 cc of water. At the end of this addition, the agitation is continued for 15 minutes and the above indoaniline which has precipitated is then filtered, washed with water, recrystallized in a mixture of dimethylformamide in water and dried under a vacuum. It exhibits a melting point of 226° C.

後処理

  1. customThe resulting reaction mixture
  2. additionthere are introduced simultaneously, with good agitation and with the aid of a double funnel
  3. additionAt the end of this addition
  4. customthe above indoaniline which has precipitated
  5. filtrationis then filtered
  6. washwashed with water
  7. customrecrystallized in a mixture of dimethylformamide in water
  8. customdried under a vacuum

出典と根拠

ORDレコード
ord-4a7cea257bc9420e9612f16fff1bd406
出典データセット
uspto-grants-1981_02
特許番号
US04248591

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