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

HRID 2425526Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2425526
[CH2:1]([NH2:4])[CH:2]=[CH2:3].Cl[CH2:6][Si:7]([CH3:10])([CH3:9])[CH3:8].[OH-].[Na+]>O>[CH3:6][Si:7]([CH2:10][NH:4][CH2:1][CH:2]=[CH2:3])([CH3:9])[CH3:8]

Komponenten

5

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

Allylamine (29.5 ml, 392.5 mmol) was warmed to 40° C. under nitrogen atmosphere. Chloromethyltrimethylsilane (25.0 ml, 180 mmol) was added very slowly to the allylamine while stirring. After the addition was complete the mixture was warmed to 70° C. for 24 hours. The mixture was cooled to 0° C. and water (25 ml) was added, followed by 2 N NaOH solution (75 ml). The mixture was stirred for one hour and was then extracted with tert-butyl methyl ether (tBME; 2×100 ml). The organic layer was dried with Na2SO4 and then concentrated under vacuum at 300 mbar at 70° C. to give pure N-((trimethylsilyl)methyl)prop-2-en-1-amine (21 g, 146.5 mmol) in 81% c.y.

Aufarbeitung

  1. additionAfter the addition
  2. temperatureThe mixture was cooled to 0° C.
  3. stirringThe mixture was stirred for one hour
  4. extractionwas then extracted with tert-butyl methyl ether (tBME; 2×100 ml)
  5. dry with materialThe organic layer was dried with Na2SO4
  6. concentrationconcentrated under vacuum at 300 mbar at 70° C.

Quellen und Nachweise

ORD-Eintrag
ord-a2a3022960dc45328e3304b28f3dc2ac
Quelldatensatz
uspto-grants-2011_06
Patentnummer
US07964739B2

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