Reaktion #2122471

Reaktionsgleichung

Calcium carbonate

Dimethylcarbamyl chloride

N-octyl acetamide

sodium hydroxide

→

product

Ausbeute 53.0%

N,N-Dimethyl-N′-heptyl Ethanimidamide

Ausbeute 53.0%

Lösungsmittel

toluene

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturthe solution was refluxed under a nitrogen atmosphere for 16 h
2. 2
   SonstigeThe volatile materials were removed on a rotary evaporator in vacuo
3. 3
   workup.DISSOLUTIONThe residue, dissolved 30 mL of dichloromethane
4. 4
   SonstigeThe organic phase was separated
5. 5
   Extraktionthe aqueous phase was extracted with dichloromethane (30 mL×3)
6. 6
   TrocknenThe combined organic phases were dried (calcium carbonate)
7. 7
   Sonstigethe solvent was removed on a rotary evaporator
8. 8
   workup.DISTILLATIONThe residue was distilled at 63-64° C./0.25 Torr

Vorschrift

Dimethylcarbamyl chloride (6.86 g, 63.7 mmol) was added slowly to 10.0 g (63.7 mmol) of N-octyl acetamide in 10 mL of dry toluene and the solution was refluxed under a nitrogen atmosphere for 16 h. The volatile materials were removed on a rotary evaporator in vacuo. The residue, dissolved 30 mL of dichloromethane, was stirred vigorously with a solution of 2.55 g (63.7 mmol) of sodium hydroxide in 40 mL of water for 30 min. Calcium carbonate (2.55 g) was added to the mixture and stirring was continued for an additional 30 min. The organic phase was separated and the aqueous phase was extracted with dichloromethane (30 mL×3). The combined organic phases were dried (calcium carbonate) and the solvent was removed on a rotary evaporator. The residue was distilled at 63-64° C./0.25 Torr to yield 6.2 g (53%) of product (purity 99% by GC). IR 2956, 2925, 2854 (C—H), 1626 (N═C) cm−1. 1H NMR 3.17 (t, 2H, JHH 7.5 Hz, —CH2—N═), 2.86 (s, 6H, —N—(CH3)2); 1.87 (s, 3H, —N═C(CH3)—N); 1.5 (m, 2H, —CH—CH2—N═); 1.25-1.4 (m, 10H, CH3—(CH2)5—); 0.88 (t, 3H, JHH 7.2 Hz, CH3).

Quelle