1,2-Dichloroethane → 3-(2-Chloroethyl)-5,5-dimethylimidazolidine-2,4-dione

HRID 268027

反応式

HRID 268027 の反応式
[CH3:1][C:2]1([CH3:9])[NH:6][C:5](=[O:7])[NH:4][C:3]1=[O:8].C(=O)([O-])[O-].[K+].[K+].[Cl:16][CH2:17][CH2:18]Cl>CN(C)C=O>[Cl:16][CH2:17][CH2:18][N:4]1[C:3](=[O:8])[C:2]([CH3:9])([CH3:1])[NH:6][C:5]1=[O:7]

参加物

5

反応物 3

HCID 111,2-DichloroethaneHCID 6491DimethylhydantoinHCID 11430Potassium Carbonate

生成物 1

HCID 2980853-(2-Chloroethyl)-5,5-dimethylimidazolidine-2,4-dione

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of 1,664 g of 5,5-dimethyl-hydantoin (13.0 mols), 897 g of anhydrous potassium carbonate (6.5 mols), 5,148 g of 1,2-dichloroethane (52 mols) and 1,458 ml of dimethylformamide is reacted for 18 hours and 20 minutes at 90°C to 100°C internal temperature (external temperature 155°C), whilst constantly removing the resulting water of reaction by azeotropic circulatory distillation. Water of reaction eliminated: 110 g (94.0% of theory). Thereafter the reaction mixture, whilst still hot, is separated by filtration from the potassium chloride produced, the filtrate is concentrated on a rotary evaporator at 100°C under a waterpump vacuum and the residue is dried to constant weight at 100°C and 10-1 mm Hg.

後処理

  1. customis reacted for 18 hours and 20 minutes at 90°C to 100°C internal temperature (external temperature 155°C)
  2. customwhilst constantly removing
  3. customthe resulting water of reaction
  4. distillationby azeotropic circulatory distillation
  5. customWater of reaction
  6. customThereafter the reaction mixture, whilst still hot, is separated by filtration from the potassium chloride
  7. customproduced
  8. concentrationthe filtrate is concentrated on a rotary evaporator at 100°C under a waterpump vacuum
  9. customthe residue is dried to constant weight at 100°C

出典と根拠

ORDレコード
ord-cdd7c2dea73644fc9748ec2a52c2a368
出典データセット
uspto-grants-1976_03
特許番号
US03946034

関連ノート

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