Hydrochloric Acid → 2-(2-butoxyethoxy)-N,N-bis[2-(2-butoxyethoxy)ethyl]ethanamine

HRID 66710

反応式

HRID 66710 の反応式
[CH2:1]([O-:8])[CH2:2][O:3][CH2:4][CH2:5][CH2:6][CH3:7].[Na+].Cl.Cl[CH2:12][CH2:13][N:14]([CH2:18][CH2:19]Cl)[CH2:15][CH2:16]Cl.Cl>>[CH2:13]([N:14]([CH2:18][CH2:19][O:8][CH2:1][CH2:2][O:3][CH2:4][CH2:5][CH2:6][CH3:7])[CH2:15][CH2:16][O:8][CH2:1][CH2:2][O:3][CH2:4][CH2:5][CH2:6][CH3:7])[CH2:12][O:8][CH2:1][CH2:2][O:3][CH2:4][CH2:5][CH2:6][CH3:7]

参加物

4

反応物 3

HCID 313Hydrochloric AcidHCID 61220Tris(2-chloroethyl)amine hydrochlorideHCID 23671990Sodium 2-butoxyethanolate

生成物 1

HCID 41020232-(2-butoxyethoxy)-N,N-bis[2-(2-butoxyethoxy)ethyl]ethanamine

反応条件

温度
130 °C

実験手順

When all of the water of the reaction has been eliminated, 55 g of tris(2-chloroethyl)amine hydrochloride are introduced. The mixture is heated at 130° C. for 5 hours, then cooled. Excess sodium alcoholate is then neutralized with a 10% aqueous solution of hydrochloric acid. The 3-oxaheptan-1-ol is removed by distillation and the sodium chloride is removed by filtration. The desired product, tris(3,6-dioxadecyl)amine, is distilled (192° C. under 0.1 mmHg).

後処理

  1. temperaturecooled
  2. customThe 3-oxaheptan-1-ol is removed by distillation
  3. customthe sodium chloride is removed by filtration
  4. distillationThe desired product, tris(3,6-dioxadecyl)amine, is distilled (192° C. under 0.1 mmHg)

出典と根拠

ORDレコード
ord-5377dfd8cac4454ea970e3feec082f2e
出典データセット
uspto-grants-1982_08
特許番号
US04343745

関連ノート

読み込み中…