Reacción #65578

ord-069948283b3d4279a8788d321279719a

Disolventes

Condiciones de reacción

Temperatura
55°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturais maintained for 4 hours
  2. 2
    Extracciónis extracted with hexane
  3. 3
    Extracciónis extracted (2 times) with ethyl ether
  4. 4
    LavadoThe combined ethereal extracts are washed with 1N hydrochloric acid
  5. 5
    Secadoare dried over magnesium sulfate
  6. 6
    FiltraciónFiltration and evaporation
  7. 7
    Otrogives 7.48 g of crude title compound
  8. 8
    OtroRecrystallization of a portion of the product from hexane

Procedimiento

To a solution of 7.6 g (30 mmol) of methyl 3-cyclododecylpropanoate in 100 ml of methanol is added 2.4 g of sodium hydroxide. The mixture is heated to 55° C. and is maintained for 4 hours. The reaction mixture is diluted with water and is extracted with hexane. The aqueous phase is acidified with 1N hydrochloric acid and is extracted (2 times) with ethyl ether. The combined ethereal extracts are washed with 1N hydrochloric acid and are dried over magnesium sulfate. Filtration and evaporation gives 7.48 g of crude title compound. Recrystallization of a portion of the product from hexane gives 1.81 g of the title compound: m.p. 72°-74° C.; IR (KBr) 1715 cm-1 ; NMR (CDCl3) δ 1.34 (m, 23H), 1.57 (q, 2H, J=8 Hz), 2.36 (t, 2H, J=8 Hz). Anal. Calc'd. for C15H28O2 : C, 74.95;H, 11.74; Found: C, 74.90;H, 11.20.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05420153uspto-grants-1995_05