Реакция #366244

ord-2a0aa955bf4f45e48947f45cd21b619f

Уравнение реакции

CCOB(OCC)OCC
triethyl borate
Cc1ccc(Br)c(OC(C)C)c1
3-isopropoxy-4-bromotoluene
C1CCOC1
tetrahydrofuran
[Li][CH2]CCC
butyl lithium
Cc1ccc(B(O)O)c(OC(C)C)c1
2-Isopropoxy-4-methylphenylboronic Acid

Растворители

Условия реакции

Температура
-70°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеTo a 125 mL 3N round-bottomed flask equipped with N2 inlet
  2. 2
    workup.STIRRINGby stirring for 5 minutes at −70° C.
  3. 3
    workup.STIRRINGstirring at room temperature for 24 hours
  4. 4
    ДругоеThe reaction was quenched with 1 N aqueous hydrochloric acid
  5. 5
    Экстракцияextracted into ethyl acetate
  6. 6
    ПромывкаThe organic layer was washed with water and brine
  7. 7
    Сушкаdried over sodium sulfate
  8. 8
    Другоеevaporated
  9. 9
    ДругоеThe residue was triturated with hexane to a white solid, 1.7 g (56%)

Методика

To a 125 mL 3N round-bottomed flask equipped with N2 inlet and septum were added 3.59 g (15.7 mmol) 3-isopropoxy-4-bromotoluene and 30 mL dry tetrahydrofuran. The solution was cooled to −70° C. and 7.5 mL (18.8 mmol) of a 2.5 M solution of butyl lithium in hexane was added over 5 minutes, and the solution stirred 5 minutes at −70° C. Then 3.2 mL (18.8 mmol) triethyl borate was added, followed by stirring for 5 minutes at −70° C. and then stirring at room temperature for 24 hours. The reaction was quenched with 1 N aqueous hydrochloric acid and extracted into ethyl acetate. The organic layer was washed with water and brine, dried over sodium sulfate, and evaporated. The residue was triturated with hexane to a white solid, 1.7 g (56%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06362195B1uspto-grants-2002_03