Réaction #9360

ord-37e41d6c8bde4a8c90ee4691de966a73

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurebefore re-cooling to −78° C.
  2. 2
    Autrebefore aqueous quench
  3. 3
    AutreThe product was purified by chromatography on SiO2 with 10% EtOAc

Mode opératoire

A solution of LDA (33 ml, 1.5 M in Et2O) in THF (50 mL) at −78° C. was treated with 4-(2-benzyloxy-ethyl)-cyclohexanone (9.5 g, 40.2 mmol). The mixture was warmed to 0° C. over 30 min. before re-cooling to −78° C. and adding HMPA (7 mL). Methyl cyanoformate (CNCO2Me, 4.1 mL, 85 mmol) was added and the mixture was stirred for 15 m before aqueous quench and work-up. The product was purified by chromatography on SiO2 with 10% EtOAc:Hx. 5-(2-Benzyloxy-ethyl)-2-oxo-)cyclohexanecarboxylic acid methyl ester was isolated, 5.8 g (49%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07091232B2uspto-grants-2006_08