Реакция #4524

ord-3c480d95de8546edb218b0eba0488c82

Уравнение реакции

CC(Cl)OC(=O)Cl
1-chloroethylchloroformate
CC1(C)Cc2cccc(O)c2O1
2,3-dihydro-2,2-dimethyl-7-benzofuranol
c1ccncc1
pyridine
CC(Cl)OC(=O)Oc1cccc2c1OC(C)(C)C2
1-chloroethyl 2,3-dihydro-2,2-dimethyl-7-benzofuranyl carbonate
Выход 84.0%

Растворители

Условия реакции

Температура
20°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture is cooled to between 0° and 5° C.
  2. 2
    ПромывкаThe organic phase is then washed with 2×50 ml of iced water
  3. 3
    СушкаIt is dried over magnesium sulphate
  4. 4
    Другоеthe solvent is evaporated
  5. 5
    ДругоеA yellow oil is obtained which
  6. 6
    workup.DISTILLATIONis distilled
  7. 7
    Другое34.1 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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04725680uspto-grants-1988_02