Реакция #330034

ord-67dc41b91d994387a499aa7bd5b42c22

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGStirring at 20° C.
  2. 2
    workup.WAITwas continued for 16 h
  3. 3
    Концентрированиеvolatiles were concentrated in vacuo
  4. 4
    ДругоеThe crude reaction mixture
  5. 5
    Другоеwas purified by column chromatography (Si—PCC, gradient 0-20% DCM in cyclohexane)

Методика

DIAD (556 mg, 2.75 mmol) was added to a solution of triphenylphosphine (722 mg, 2.75 mmol) in dioxane (5 mL) at 0° C. under a nitrogen atmosphere. After 10 min stirring, 1-(3-phenylbenzo[b]thiophen-2-yl)ethanol (350 mg, 1.37 mmol) was added followed by diphenylphosphoryl azide (454 mg, 1.65 mmol). Stirring at 20° C. was continued for 16 h and then volatiles were concentrated in vacuo. The crude reaction mixture was purified by column chromatography (Si—PCC, gradient 0-20% DCM in cyclohexane) affording 2-(1-Azidoethyl)-3-phenylbenzo[b]thiophene as a colourless oil (211 mg, 55%). 1H NMR (CDCl3, 400 MHz): δ 7.88 (1H, d, J=7.87 Hz), 7.54-7.42 (4H, m), 7.41-7.29 (4H, m), 4.97 (1H, q, J=6.80 Hz), 1.58 (3H, d, J=6.80 Hz).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08653089B2uspto-grants-2014_02