反応式
[CH3:1][N:2]([CH2:4][CH2:5][CH2:6][NH2:7])[CH3:3].[CH2:8]([NH2:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH2:16]([CH:18]1[O:20][CH2:19]1)[Cl:17].C(O)=O>O>[CH2:16]([CH:18]1[O:20][CH2:19]1)[Cl:17].[CH3:1][N:2]([CH2:4][CH2:5][CH2:6][NH2:7])[CH3:3].[CH2:8]([NH2:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1参加物
6
反応条件
- 温度
- 50 °C
実験手順
1 020 g (10 mol) of dimethylaminopropylamine and 267.5 g (2.5 mol) of benzylamine are mixed in 1 519.1 g of water. The solution/suspension is heated to 50° C. Thereafter, 931 ml of epichlorohydrin (1 098.4 g/l 1.875 mol) are added dropwise at a rate of 16 ml/min while heating to 85° C., and stirring is effected for two hours at 85° C. The stirring at 85° C. is continued until free alkylating agent is no longer detectable (Preuβmann test). The reaction mixture is cooled, diluted with 2 l of water and brought to a pH of 7.0 with 85% strength formic acid. Further water is added until the solids content is 21%.
後処理
- temperaturewhile heating to 85° C.
- customstirring at 85° C.
- temperatureThe reaction mixture is cooled
出典と根拠
- ORDレコード
- ord-4d438631632e491eab1ba9bb43893932
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07728072B2
関連ノート
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