Реакция #2122472

ord-7af00617a07b4d7ab01a422286f00e26

Уравнение реакции

O=C([O-])[O-].[Ca+2]
Calcium carbonate
CN(C)C(=O)Cl
Dimethylcarbamyl chloride
CCCCCCCCNC(C)=O
N-octyl acetamide
[Na+].[OH-]
sodium hydroxide
CCCCCCCCN=C(C)N(C)C
product
Выход 61.3%
CCCCCCCCN=C(C)N(C)C
N,N-Dimethyl-N′-octyl Ethanimidamide
Выход 61.3%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe solution was refluxed under a nitrogen atmosphere for 16 h
  2. 2
    ДругоеThe volatile materials were removed on a rotary evaporator and in vacuo
  3. 3
    workup.DISSOLUTIONThe residue, dissolved dichloromethane (30 mL)
  4. 4
    ДругоеThe organic phase was separated
  5. 5
    Промывкаthe aqueous phase was washed with dichloromethane (30 mL×3)
  6. 6
    СушкаThe combined organic phases were dried (calcium carbonate)
  7. 7
    Другоеthe volatile materials were removed on a rotary evaporator
  8. 8
    workup.DISTILLATIONThe residue was distilled at 72-77° C./0.25 Torr

Методика

Dimethylcarbamyl chloride (6.29 g, 58.4 mmol) was added slowly to 10.0 g (58.4 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 and in vacuo. The residue, dissolved dichloromethane (30 mL), was stirred strongly for 30 min with a solution of 2.34 g (58.4 mmol) of sodium hydroxide in 40 mL of water. Calcium carbonate (2.34 g) was added to the mixture and it was stirred an additional 30 min. The organic phase was separated and the aqueous phase was washed with dichloromethane (30 mL×3). The combined organic phases were dried (calcium carbonate) and the volatile materials were removed on a rotary evaporator. The residue was distilled at 72-77° C./0.25 Torr to yield 7.1 g (61%) of product (purity 99% by GC). IR (neat) 2955, 2924, 2853 (C—H), 1627 (N═C) cm−1. 1H NMR 3.17 (t, 2H, JHH 6.9 Hz, —CH2—N═), 2.86 (s, 6H, —N—(CH3)2); 1.87 (s, 3H, —N═C(CH3)—N); 1.5 (m, 2H, —CH2—CH2—N═); 1.25-1.4 (m, 10H, CH3—(CH2)5—); 0.88 (t, 3H, JHH 6.1 Hz, CH3).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08574453B2uspto-grants-2013_11