Реакция #162013

ord-e37202d94ea64e499d0f22ef85793fe5

Уравнение реакции

OCCCCCCCCCCCCBr
12-bromo-1-dodecanol
[N-]=[N+]=[N-].[Na+]
sodium azide
O=C([O-])O.[Na+]
sodium bicarbonate
[N-]=[N+]=NCCCCCCCCCCCCO
12-Azido-1-dodecanol
Выход 92.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe mixture was filtered through a plug of celite
  2. 2
    Промывкаthe cake rinsed with ethyl acetate (20 mL)
  3. 3
    ДругоеThe combined filtrate and washings were evaporated onto silica gel
  4. 4
    Другоеpurified by flash column (2.5×18 cm, gradient elution with hexane-ethyl acetate 6:1, 4:1 to 2:1)

Методика

A mixture of 12-bromo-1-dodecanol (246 mg, 0.927 mmol) in t-butanol (1.8 mL, 0.5 M) was treated with sodium azide (121 mg, 1.855 mmol, 2 eq), tetrabutylammonium iodide (17 mg, 0.0464 mmol, 0.05 eq) and sat. aq. sodium bicarbonate solution (0.9 mL) in that order. The mixture was stirred at room temperature for 4 days. The mixture was filtered through a plug of celite and the cake rinsed with ethyl acetate (20 mL). The combined filtrate and washings were evaporated onto silica gel and purified by flash column (2.5×18 cm, gradient elution with hexane-ethyl acetate 6:1, 4:1 to 2:1) to give 12-Azido-1-dodecanol as a colourless oil (193 mg, 92%). 1H NMR (CDCl3, 400 MHz): 3.62 (t, 2H, J=7.0, OCH2), 3.24 (t, 2H, J=7.0, NCH2), 1.61-1.51 (m, 4H), 1.35-1.25 (m, 16H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08828952B2uspto-grants-2014_09