Реакция #1435720

ord-a4528f76be924b91a658fcb1b32c97a0

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction is maintained
  2. 2
    Экстракцияthe organic phase is extracted
  3. 3
    Концентрированиеconcentrated to dryness in order
  4. 4
    Другоеto give an orange oil

Методика

To 50 ml of a 2.3 M solution of sodium cyclopentadienylide (115 mmol), a solution of 24.3 g (115 mmol) of 3-bromo-1-trimethylsiloxypropane in tetrahydrofurane is added. The quick formation of a pinkish solid is observed. The reaction is maintained under stirring for 12 hours and then it is neutralised with an ammonium chloride solution; the organic phase is extracted and concentrated to dryness in order to give an orange oil. (9.8 g, 50 mmol. Yield: 43%). 1H-NMR (CDCl3): 6.47–6.00 (m, 3H), 3.62 (m, 2H), 2.95 (m, 1H), 2.87 (m, 1H), 2.43 (m, 2H), 1.80 (m, 2H), 0.17 (s, 9H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07211538B2uspto-grants-2007_05