Реакция #1256712

ord-2467e9484284466b8569b1cbf6b9a770

Уравнение реакции

[Al]
aluminum
Cc1cncc(C)c1-c1c(C)cc(N)cc1C
10
Cc1cncc(C)c1-c1c(C)cc(N)cc1C
4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenylamine
F[B-](F)(F)F.N#[O+]
nitrosonium tetrafluoroborate
[I-].[Na+]
NaI
O=S([O-])([O-])=S.[Na+].[Na+]
Na2S2O3
Cc1cncc(C)c1-c1c(C)cc(I)cc1C
title compound
Выход 72.0%
Cc1cncc(C)c1-c1c(C)cc(I)cc1C
4-(4-iodo-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridine
Выход 72.0%

Растворители

Условия реакции

Температура
-30°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураto gradually warm to room temperature
  2. 2
    workup.STIRRINGstirred at room temperature overnight
  3. 3
    Экстракцияextracted with chloroform (50 mL×3)
  4. 4
    ДругоеThe organic layer was separated
  5. 5
    Сушкаdried over anhydrous Na2SO4
  6. 6
    Фильтрацияfiltered
  7. 7
    Концентрированиеconcentrated in vacuo
  8. 8
    ДругоеThe crude product was purified by flash chromatography on silica gel
  9. 9
    Промывкаeluting with 8:1 chloroform

Методика

To a stirring suspension of nitrosonium tetrafluoroborate (0.876 g, 7.50 mmol) in dry acetonitrile (10 mL) was added dropwise via syringe a solution of 10 (0.904 g, 4.00 mmol) in dry acetonitrile (15 mL) under N2 at −30° C. The reaction mixture was next stirred at −30° C. for 1 h. To the resulting yellow solution was then added dropwise in the dark a solution of anhydrous NaI (1.125 g, 7.50 mmol) in dry acetonitrile (10 mL) under N2 at −30° C. The reaction mixture was covered with aluminum foil, allowed to gradually warm to room temperature, and stirred at room temperature overnight. The resulting red solution was next decolorized using an aqueous solution of Na2S2O3 and extracted with chloroform (50 mL×3). The organic layer was separated, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel, eluting with 8:1 chloroform: ethyl acetate, to give 0.96 g (72%) of the title compound as a yellow solid: mp 242-243° C.; 1H NMR (400 MHz, CDCl3): δ 8.397 (s, 2H), 7.520 (s, 2H), 1.908 (s, 6H), 1.838 (s, 6H); 13C NMR (100 MHz, CDCl3): δ 148.611, 147.520, 136.983, 136.774, 130.841, 93.681, 19.488, 16.758; MS(ESI): m/z 338.2[(M+H)+, 100]; Anal. Calcd. for C15H16IN: C, 53.43; H, 4.78; N, 4.15. Found; C, 52.91; H, 4.72; N, 4.07.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07824582B2uspto-grants-2010_11