Реакция #69210

ord-2a2460e85366466f80ca7c20c4ed767a

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThis was partitioned between ethyl acetate and brine
  2. 2
    ПромывкаThe organic layer was washed with brine
  3. 3
    Сушкаdried over magnesium sulfate
  4. 4
    Концентрированиеconcentrated

Методика

The 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.10 g, 0.00052 mol) was combined with naphthalene, 2-(bromomethyl)- (0.12 g, 0.00057 mol) in ACN (3.0 mL, 0.057 mol) under nitrogen at rt. Then cesium carbonate (0.50 g, 0.0015 mol) was added and the reaction was complete after stirring for 1 h. This was partitioned between ethyl acetate and brine. The organic layer was washed with brine, dried over magnesium sulfate and concentrated to give 1-(2-naphthylmethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole 0.17 gm, as an oil, LC/MS (M+H)+: 335, 1H NMR (CDCl3) δ 7.89 (s, 1H), 7.79-7.84(m, 3H), 7.69(bs, 2H), 7.49-7.4(m, 2H), 7.46-7.33(m, 1H), 5.47(s, 2H), 1.31(s, 12H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08530485B2uspto-grants-2013_09