Reacción #1605782
ord-a51f7b88efa945389ef2ed4bcecd4c88
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otroto come to ambient temperature
- 2Otroquenched with water
- 3OtroAfter separation of the phases
- 4Extracciónthe water phase was extracted once with dichlormethane
- 5Concentraciónthe combined organic phases were concentrated
- 6workup.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%.