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Ethylenediamine → N,N'-Bis(3-(trimethoxysilyl)propyl)ethane-1,2-diamine

HRID 867374
ノート
印刷プレビュー

反応式

HRID 867374 の反応式
[NH2:1][CH2:2][CH2:3][NH:4][CH2:5][CH2:6][CH2:7][Si:8]([O:13][CH3:14])([O:11][CH3:12])[O:9][CH3:10].Cl[CH2:16][CH2:17][CH2:18][Si:19]([O:24][CH3:25])([O:22][CH3:23])[O:20][CH3:21].C(N)CN>>[Si:8]([CH2:7][CH2:6][CH2:5][NH:4][CH2:3][CH2:2][NH:1][CH2:16][CH2:17][CH2:18][Si:19]([O:24][CH3:25])([O:22][CH3:23])[O:20][CH3:21])([O:13][CH3:14])([O:9][CH3:10])[O:11][CH3:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 3301EthylenediamineHCID 15659(Trimethoxysilylpropyl)ethylenediamineHCID 624493-(Trimethoxysilyl)propyl chloride2 回

生成物 1

HCID 111651N,N'-Bis(3-(trimethoxysilyl)propyl)ethane-1,2-diamine収率 972.3%

反応条件

温度
140 °C

実験手順

A 2 liter, 3-necked reaction flask equipped with a magnetic stirrer, electric heating mantle, dropping funnel and water condenser, containing 22.0 grams of NH2CH2CH2NH(CH2)3Si(OCH3)3 was heated to 140° C. whereupon the addition thereto of 198.0 grams of 3-chloropropyltrimethoxy silane (Cl(CH2)3Si(OCH3)3) was commenced. Cl(CH2)3Si(OCH3)3 was introduced dropwise to the reaction flask over a period of 1 hour while maintaining a temperature of 145° C. to 150° C. by the occasional application of a water bath. The resultant mixture was cooled to 75° C., and 90 grams of anhydrous ethylenediamine was added to the cooled mixture. Thereafter, the mixture was allowed to separate into layers with the upper product containing layer being separated therefrom and stripped by vacuum distillation of lowboiling volatiles to yield 370 grams of (CH3O)3SiC3H6NHC2H4NHC3H6Si(OCH3)3. Amine titration and 13C NMR and 29Si NMR analysis verified the assigned structure of the resultant product.

後処理

  1. customA 2 liter, 3-necked reaction flask equipped with a magnetic stirrer
  2. temperaturewhile maintaining a temperature of 145° C. to 150° C. by the occasional application of a water bath
  3. customto separate into layers with the upper product
  4. additioncontaining layer
  5. custombeing separated
  6. distillationstripped by vacuum distillation of lowboiling volatiles

出典と根拠

ORDレコード
ord-513f8d27df4b4f80b49d229d66d95064
出典データセット
uspto-grants-1988_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04775415

反応ノート

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