Réaction #2122470

Équation de réaction

N-hexyl acetamide

dimethylcarbamyl chloride

→

liquid

Rendement 49.0%

N,N-Dimethyl-N′-hexyl Ethanimidamide

Rendement 49.0%

Solvants

toluene

Conditions de réaction

Traitement

1. 1
   TempératureThe solution was refluxed under a nitrogen atmosphere for 24 h
2. 2
   AutreThe volatile materials were removed on a rotary evaporator
3. 3
   Autreat room temperature
4. 4
   workup.DISSOLUTIONThe residue was dissolved 30 mL of chloroform
5. 5
   workup.ADDITIONCalcium carbonate (4.2 g) was added
6. 6
   workup.STIRRINGstirring
7. 7
   workup.WAITwas continued for another 30 min
8. 8
   AutreThe organic phase was separated
9. 9
   Extractionthe aqueous phase was extracted with dichloromethane (25 mL×3)
10. 10
    SéchageThe combined organic phases were dried (calcium carbonate)
11. 11
    Autrethe solvent was removed on a rotary evaporator
12. 12
    workup.DISTILLATIONThe residue was distilled at 52-54° C./0.25 Torr (lit. bp 125° C./30 Torr (see Oszczapowicz, J.; Raczynska, E. J. Chem. Soc., Perkin Trans. 2 1984, 1643-1666)) product

Mode opératoire

To a solution of N-hexyl acetamide (15.0 g, 105 mmol) in 15 mL of dry toluene was slowly added 11.2 g (104.9 mmol) of dimethylcarbamyl chloride. The solution was refluxed under a nitrogen atmosphere for 24 h. The volatile materials were removed on a rotary evaporator and then in vacuo at room temperature. The residue was dissolved 30 mL of chloroform and stirred vigorously with a solution of 4.2 g sodium hydroxide in 40 mL of water for 30 min. Calcium carbonate (4.2 g) was added and stirring was continued for another 30 min. The organic phase was separated and the aqueous phase was extracted with dichloromethane (25 mL×3). The combined organic phases were dried (calcium carbonate) and the solvent was removed on a rotary evaporator. The residue was distilled at 52-54° C./0.25 Torr (lit. bp 125° C./30 Torr (see Oszczapowicz, J.; Raczynska, E. J. Chem. Soc., Perkin Trans. 2 1984, 1643-1666)) product to yield 8.7 g (49%) of liquid (purity 99% by GC). IR (neat) 2955, 2926, 2856 (C—H), 1626 (N═C) cm−1. 1H NMR 3.18 (t, 2H, JHH 7.5 Hz, —CH2—N═), 2.87 (s, 6H, —N—(CH3)2); 1.87 (s, 3H, —N═C(CH3)—N); 1.49 (m, 2H, —CH2—CH2—N═); 1.25-1.4 (m, 6H, CH3—(CH2)3—); 0.88 (t, 3H, JHH 7.2 Hz, CH3). 13C NMR 158.79; 50.32; 38.07; 32.49; 32.00; 27.38; 22.80; 14.17; 12.45.

Source