Reacción #2122469

ord-280b7033ef3b4cd1a58a8d3732f7f24b

Ecuación de reacción

[Na+].[OH-]
sodium hydroxide
CN(C)C(=O)Cl
dimethylcarbamyl chloride
O=C([O-])[O-].[Ca+2]
Calcium carbonate
CCCCCCNC(C)=O
N-Hexyl acetamide
CCCCCN=C(C)N(C)C
product
Rendimiento 38.8%
CCCCCN=C(C)N(C)C
N,N-Dimethyl-N′-amyl ethanimidamide
Rendimiento 38.8%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturarefluxed under a nitrogen atmosphere for 16 h
  2. 2
    OtroThe volatile materials were removed on a rotary evaporator
  3. 3
    Otroat room temperature
  4. 4
    workup.ADDITIONwas added
  5. 5
    workup.STIRRINGwas stirred another 30 min
  6. 6
    OtroThe organic phase was separated
  7. 7
    Lavadothe aqueous phase was washed with dichloromethane (3×25 mL)
  8. 8
    SecadoThe combined organic liquids were dried (calcium carbonate)
  9. 9
    Otrothe volatile materials were removed on a rotary evaporator
  10. 10
    workup.DISTILLATIONThe residue was distilled at 40-41° C./0.25 Torr

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08574453B2uspto-grants-2013_11