反応式
[NH2:1][C:2]1[CH:7]=[C:6]([NH2:8])[CH:5]=[CH:4][C:3]=1[CH3:9].[C:10](=[O:15])([O:12][CH2:13][CH3:14])N>C(O)C>[CH2:13]([O:12][C:10]([NH:1][C:2]1[CH:7]=[C:6]([NH:8][C:10]([O:12][CH2:13][CH3:14])=[O:15])[CH:5]=[CH:4][C:3]=1[CH3:9])=[O:15])[CH3:14]参加物
4
実験手順
275 g of a polyurea mixture based on 2,4-diamino-toluene having terminal amino tolyl groups (average molecular weight: 1500) were introduced into the apparatus described in Example 1. 513 g of 2,4-diamino-toluene, 933 g ethyl carbamate and 1250 g ethanol (approximately 96%) were subsequently added. The mixture was reacted for 6.0 hours at 200° C. After the apparatus had cooled and the pressure had been reduced, the reaction mixture was removed, filtered and analyzed by high pressure liquid chromatography (HPLC). A yield of 1100 g (68% of the theoretical yield) of 2,4-bis-(ethoxy carbonylamino)-toluene was obtained.
後処理
- additionwere introduced into the apparatus
- customThe mixture was reacted for 6.0 hours at 200° C
- temperatureAfter the apparatus had cooled
- customthe reaction mixture was removed
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-d00f46fb57034a189dbb0a132ce18804
- 出典データセット
- uspto-grants-1983_06
- 特許番号
- US04388238
関連ノート
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