Reaktion #2122469
ord-280b7033ef3b4cd1a58a8d3732f7f24b
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturrefluxed under a nitrogen atmosphere for 16 h
- 2SonstigeThe volatile materials were removed on a rotary evaporator
- 3Sonstigeat room temperature
- 4workup.ADDITIONwas added
- 5workup.STIRRINGwas stirred another 30 min
- 6SonstigeThe organic phase was separated
- 7Waschenthe aqueous phase was washed with dichloromethane (3×25 mL)
- 8TrocknenThe combined organic liquids were dried (calcium carbonate)
- 9Sonstigethe volatile materials were removed on a rotary evaporator
- 10workup.DISTILLATIONThe residue was distilled at 40-41° C./0.25 Torr
Vorschrift
N-Hexyl acetamide (10.0 g, 77.5 mmol) was added 10 mL of dry toluene, then 8.33 g (77.5 mmol) of dimethylcarbamyl chloride was slowly added and then refluxed under a nitrogen atmosphere for 16 h. The volatile materials were removed on a rotary evaporator and then in vacuo at room temperature. The residue was dissolved dichloromethane (30 mL) and 3.1 g (77.5 mmol) of sodium hydroxide dissolved aqueous solution (40 mL) was added. The mixture was stirred vigorously for 30 min. Calcium carbonate (3.1 g) was added to the mixture and it was stirred another 30 min. The organic phase was separated and the aqueous phase was washed with dichloromethane (3×25 mL). The combined organic liquids were dried (calcium carbonate) and the volatile materials were removed on a rotary evaporator. The residue was distilled at 40-41° C./0.25 Torr to yield 4.7 g (39%) of product (98.5% pure by GC). IR (neat) 2956, 2927, 2857 (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); 1.88 (s, 3H, —N═C(CH3)—N); 1.51 (m, 2H, —CH—CH2—N═); 1.25-1.4 (m, 4H, CH3—(CH2)2—); 0.90 (t, 3H, JHH 6.9 Hz, CH3). 13C NMR 158.90; 50.35; 38.15; 32.27; 29.98; 22.87; 14.31; 12.53.