Carbamic acid, ethyl ester → Diethyl toluene-2,4-dicarbamate

HRID 128465

反応式

HRID 128465 の反応式
[NH2:1][C:2]([O:4][CH2:5][CH3:6])=[O:3].[Mn]([O-])(=O)(=O)=O.[K+].C[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][C:19]=1[CH3:20]>>[CH2:5]([O:4][C:2]([NH:1][C:18]1[CH:17]=[C:16]([NH:1][C:2]([O:4][CH2:5][CH3:6])=[O:3])[CH:15]=[CH:14][C:19]=1[CH3:20])=[O:3])[CH3:6]

参加物

4

反応条件

温度
80 °C

実験手順

10 g of the urethane which had previously been treated in this way were dissolved in 60 g o-xylene. The solution is heated to 80° C. and mixed with 2 g of a 2%, by weight, aqueous potassium permanganate solution. The mixture was stirred intensely for 30 minutes at 80° C. The hot organic phase was then separated from the solid and aqueous constituents. The organic phase was concentrated by distilling off a proportion of the xylene to half of its original volume, and the purified 2,4-bis-(ethoxycarbonylamino)-toluene was obtained in a virtually quantitative yield from the concentrated solution by crystallization.

後処理

  1. customThe hot organic phase was then separated from the solid and aqueous constituents
  2. concentrationThe organic phase was concentrated
  3. distillationby distilling off a proportion of the xylene to half of its original volume

出典と根拠

ORDレコード
ord-2434c732e1b74e2095af672870efccea
出典データセット
uspto-grants-1981_03
特許番号
US04259511

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