Реакция #4524
ord-3c480d95de8546edb218b0eba0488c82
Уравнение реакции
1-chloroethylchloroformate
2,3-dihydro-2,2-dimethyl-7-benzofuranol
pyridine
→
1-chloroethyl 2,3-dihydro-2,2-dimethyl-7-benzofuranyl carbonate
Выход 84.0%
Реагенты
Нет
Растворители
Условия реакции
Температура
20°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ТемператураThe mixture is cooled to between 0° and 5° C.
- 2ПромывкаThe organic phase is then washed with 2×50 ml of iced water
- 3СушкаIt is dried over magnesium sulphate
- 4Другоеthe solvent is evaporated
- 5ДругоеA yellow oil is obtained which
- 6workup.DISTILLATIONis distilled
- 7Другое34.1 g of the expected carbonate is then recovered (84% yield)
Методика
21.5 g (0.15 mole) of 1-chloroethylchloroformate are added in a single portion to a solution of 2,3-dihydro-2,2-dimethyl-7-benzofuranol (24.6 g; 0.15 mole) in dichloromethane (150 ml). The mixture is cooled to between 0° and 5° C., and 12 g (0.15 mole) of pyridine are added dropwise. The mixture is stirred for 3 hours at 20° C. The organic phase is then washed with 2×50 ml of iced water. It is dried over magnesium sulphate and the solvent is evaporated. A yellow oil is obtained which is distilled. 34.1 g of the expected carbonate is then recovered (84% yield).