Allylamine → N-((trimethylsilyl)methyl)prop-2-en-1-amine

HRID 380467ノート

反応式

HRID 380467 の反応式
[CH2:1]([NH2:4])[CH:2]=[CH2:3].Cl[CH2:6][Si:7]([CH3:10])([CH3:9])[CH3:8].[OH-].[Na+]>O>[CH2:1]([NH:4][CH2:6][Si:7]([CH3:10])([CH3:9])[CH3:8])[CH:2]=[CH2:3]

参加物

5

反応条件

温度
70 °C

実験手順

To 118 mL (1.57 mol) of allylamine warmed at 40° C. in an inert atmosphere was very slowly added 100 mL (0.72 mol) of chloromethyl trimethylsilane (approximate rate of 1 mL/min). The reaction mixture was slowly warmed to 70° C. and stirred for 24 h. The reaction mixture was cooled to 0° C. and to it was added water to break tip the gel and then 300 mL of 2N NaOH solution. The reaction mixture was extracted with ether. The combined organic fractions were washed with 500 mL of sat'd NaCl solution, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was purified by distillation (bp 80-84° C. @ 100 torr) to give 75 g of the title compound.

後処理

  1. temperatureThe reaction mixture was cooled to 0° C. and to it
  2. extractionThe reaction mixture was extracted with ether
  3. washThe combined organic fractions were washed with 500 mL of sat'd NaCl solution
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated
  7. distillationThe residue was purified by distillation (bp 80-84° C. @ 100 torr)

出典と根拠

ORDレコード
ord-ca9dd621e3b44ab4a87f09928c84883d
出典データセット
uspto-grants-2001_10
特許番号
US06303593B1

反応ノート

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