Reaktion #1884992

Reaktionsgleichung

tert-butylamine

acetonitrile

tert-butyl chloride

NaOH

→

N,N′-di-tert-butyl acetamidine

Lösungsmittel

CH2Cl2

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturWhile the solution was cooled below −70° C.
2. 2
   workup.WAITThe solution was then left
3. 3
   workup.STIRRINGstirring at −70° C. for a few hours
4. 4
   Temperaturwarmed up to −20° C.
5. 5
   SonstigeThe organic layer was separated
6. 6
   Extraktionthe aqueous phase was then extracted with fresh CH2Cl2
7. 7
   WaschenCombined CH2Cl2 fractions were washed twice with water
8. 8
   Trocknendried over anhydrous MgSO4
9. 9
   SonstigeThe dried organic solution was evaporated
10. 10
    Sonstigeto yield a light yellow liquid

Vorschrift

N,N′-di-tert-butyl acetamidine was synthesized as follows. Anhydrous FeCl3 (1.04 mol.) was suspended in 1 L of CH2Cl2 under N2 at room temperature. The suspension was cooled to −40 to −50° C. and acetonitrile (1 mol) was quickly added with stirring. While the solution was cooled below −70° C., tert-butyl chloride (1.04 mol) was added, followed by tert-butylamine (1.05 mol). The solution was then left stirring at −70° C. for a few hours and then warmed up to −20° C., followed by pouring it into a diluted aqueous NaOH solution (12.5 wt %, 1 L). Additional water was added to ensure complete formation of precipitate. The organic layer was separated and the aqueous phase was then extracted with fresh CH2Cl2. Combined CH2Cl2 fractions were washed twice with water and dried over anhydrous MgSO4. The dried organic solution was evaporated to yield a light yellow liquid. The crude amidine thus obtained was then purified by fractional distillation. Yield of the main fraction was >70%, and free of organic and metallic impurities as detected by 1H NMR and ICP-MS. 1H NMR (in C6D6, δ ppm): 3.02 (br. s, 1H), 1.41 (s, 3H), δ 1.34 (s, 18H).

Quelle