Réaction #92086

ord-5d73db12900d4e17adc23f9f8043f057

Solvants

Conditions de réaction

Température
60°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureAfter cooling to RT
  2. 2
    Filtrationfiltered
  3. 3
    Autreto remove solid present at the phase interface
  4. 4
    ExtractionThe aqueous layer was extracted with MTBE (3×100 mL)
  5. 5
    LavageThe combined MTBE layers were washed with brine (100 mL)
  6. 6
    Séchagedried over MgSO4
  7. 7
    Filtrationfiltered
  8. 8
    Concentrationconcentrated by rotary evaporation

Mode opératoire

A 3-N 250 mL flask was charged with trimethyl-(6,10,14-trimethyl-pentadeca-5,9,13-trien-1-ynyl)-silane (Ex-1B-7) (19.38 g, 64.1 mmol) and NaOEt (42 mL of a 21% w/w solution, 112 mmol). The reaction mixture was stirred at 60° C. for 4 h. After cooling to RT, the reaction mixture was diluted with MTBE (100 mL) and water (100 mL) and then filtered to remove solid present at the phase interface. The aqueous layer was extracted with MTBE (3×100 mL). The combined MTBE layers were washed with brine (100 mL), dried over MgSO4, filtered, and concentrated by rotary evaporation to yield 12.43 g of 6,10,14-trimethyl-pentadeca-5,9,13-trien-1-yne (Ex-1B-8) as a dark orange oil (96%). 1H NMR (400 MHz, CDCl3) δ (ppm): 5.23-5.17 (m, 1H), 5.17-5.07 (m, 2H), 2.29-1.95 (m, 13H), 1.70 (s, 3H), 1.65 (s, 3H), 1.62 (s, 6H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09447006B2uspto-grants-2016_09