Methylamine → HCID 86643717、化合物

HRID 240233ノート

反応式

HRID 240233 の反応式
[CH2:1]([NH2:3])C.[Li]CCCC.[C:9]([Si:13]([CH2:18][CH3:19])(OC)OC)([CH3:12])([CH3:11])[CH3:10].[CH3:20][NH2:21]>CCCCCC.C1COCC1>[CH3:20][NH:21][Si:13]([NH:3][CH3:1])([C:9]([CH3:12])([CH3:11])[CH3:10])[CH2:18][CH3:19]

参加物

7

反応条件

温度
-10 °C

実験手順

A three-necked flask in which the internal atmosphere was sufficiently replaced with nitrogen gas was charged with 60 ml of a THF solution containing 0.04 mol of ethylamine in a nitrogen stream. 30 ml of a hexane solution containing 0.04 mol of BuLi was slowly added to the ethylamine solution cooled to −10° C. using a dripping funnel. After the addition, the mixture was gradually heated and reacted at 50° C. for two hours. Another container of which the internal atmosphere was purged with nitrogen was charged with 60 ml of a toluene solution containing 0.02 mol of t-butylethyldimethoxysilane and cooled to −10° C. The above slurry of Li salt of methylamine was slowly added dropwise to the cooled solution under nitrogen seal. After the addition, the mixture was reacted at 50° C. for three hours. The reaction mixture was separated into a solid and a solution by centrifugation. The solid was washed with 20 ml of toluene and added to the solution. The solvent was evaporated from the solution under reduced pressure and the residue was distilled under reduced pressure to obtain bis(methylamino)-t-butylethylsilane. The elementary analysis confirmed that the compound consists of C: 55.01% (55.11%), H: 12.57% (12.72%), and N: 16.25% (16.07%), wherein the percentages of the parentheses are theoretical values.

後処理

  1. customA three-necked flask in which the internal atmosphere was sufficiently replaced with nitrogen gas
  2. additionAfter the addition
  3. temperaturethe mixture was gradually heated
  4. customreacted at 50° C. for two hours
  5. customAnother container of which the internal atmosphere was purged with nitrogen
  6. additionwas charged with 60 ml of a toluene solution
  7. temperaturecooled to −10° C
  8. customseal
  9. additionAfter the addition
  10. customthe mixture was reacted at 50° C. for three hours
  11. customThe reaction mixture was separated into a solid
  12. washThe solid was washed with 20 ml of toluene
  13. additionadded to the solution
  14. customThe solvent was evaporated from the solution under reduced pressure
  15. distillationthe residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-f7035f472e884cb1bf85e5c4024ff7e7
出典データセット
uspto-grants-2014_02
特許番号
US08648001B2

反応ノート

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