Reacción #1605782

ord-a51f7b88efa945389ef2ed4bcecd4c88

Ecuación de reacción

c1ccncc1
pyridine
c1ccncc1
pyridine
O=C(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl
triphosgene
CCNCC
diethylamine
CC1CCC(C)C(O)C1C
2,3,6-trimethylcyclohexanol
CCN(CC)C(=O)OC1C(C)CCC(C)C1C
desired product
Rendimiento 51.8%
CCN(CC)C(=O)OC1C(C)CCC(C)C1C
Diethyl-carbamic acid 2,3,6-trimethyl-cyclohexyl ester
Rendimiento 51.8%

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto come to ambient temperature
  2. 2
    Otroquenched with water
  3. 3
    OtroAfter separation of the phases
  4. 4
    Extracciónthe water phase was extracted once with dichlormethane
  5. 5
    Concentraciónthe combined organic phases were concentrated
  6. 6
    workup.DISTILLATIONThe raw product was purified by distillation and column chromatography

Procedimiento

4.27 g (30 mmol) of 2,3,6-trimethylcyclohexanol were placed with 110 ml dichlormethane in a 250 ml vessel at room temperature and 3.08 g (39 mmol) of pyridine were added. The reaction mixture was cooled to 0° C. and 3.56 g (12 mmol) of triphosgene in 15 ml dichlormethane were added dropwise. After five minutes 2.37 g (30 mmol) pyridine were added. Subsequently, 2.19 g (30 mmol) of diethylamine in 15 ml dichlormethane were added dropwise, the resulting mixture was allowed to come to ambient temperature and then quenched with water. After separation of the phases, the water phase was extracted once with dichlormethane and the combined organic phases were concentrated. The raw product was purified by distillation and column chromatography to yield 1.5 g of the desired product as a mixture of isomers with a purity of 99.4%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09072676B2uspto-grants-2015_07