Реакция #721252

ord-2660b9f55cc64a16ab9987e7e7a8c385

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGThe resulting mixture was stirred overnight at room temperature
  2. 2
    Другоеevaporated to dryness
  3. 3
    workup.ADDITIONThe residue was poured into 500 ml of water, crude product
  4. 4
    Экстракцияwas extracted with 3×200 ml of ethyl acetate
  5. 5
    ЭкстракцияThe combined organic extract
  6. 6
    Сушкаwas dried over Na2SO4
  7. 7
    Другоеevaporated to dryness

Методика

To a solution of 35.0 g (0.19 mol) of 2,6-dimethylbromobenzene cooled to −78° C., 76 ml (0.19 mol) of 2.5 M nBuLi in hexanes was added for 40 min. The resulting mixture was stirred at this temperature for 1 h, then 35.2 g (0.19 mol) of 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane was added. The resulting mixture was stirred overnight at room temperature and then evaporated to dryness. The residue was poured into 500 ml of water, crude product was extracted with 3×200 ml of ethyl acetate. The combined organic extract was dried over Na2SO4 and then evaporated to dryness. Yield 19.5 g (53%) of yellow crystalline solid. Anal. calc. for C14H21BO2: C, 72.44; H, 9.12. Found: C, 72.78; H, 9.45. 1H NMR (CDCl3): δ 7.12 (t, J=7.7 Hz, 1H, 4-H), 6.94 (d, J=7.7 Hz, 2H, 3, 5-H), 2.40 (s, 6H, 2, 6-Me), 1.38 (s, 12H, Bpin).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09321858B2uspto-grants-2016_04