Reacción #2028896

ord-36ac30b23ff944f596ec67d93eeb3561

Ecuación de reacción

Cl
HCl
O=C1CCCCCO1
caprolactone
O=C1CCCCCO1
Caprolactone
[K+].[OH-]
potassium hydroxide
CO
methanol
O=C(O)CCCCCO
6-hydroxyhexanoic acid

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with ethyl acetate
  2. 2
    LavadoThe combined organic layers were washed with water
  3. 3
    Otrodried
  4. 4
    Filtraciónfiltered
  5. 5
    Concentraciónconcentrated

Procedimiento

First, the synthesis of Compound 20 was preformed following the procedure reported in PCT/JP2005/004389. 6-Hydroxyhexanoic acid was synthesized by base hydrolysis of caprolactone. Caprolactone (100 g) was added to a mixture of potassium hydroxide (145 g), methanol (110 mL), and THF (390 mL). The resulting mixture was stirred at room temperature overnight. The solution was then acidified with HCl and extracted with ethyl acetate. The combined organic layers were washed with water, dried, filtered, and concentrated to obtain 6-hydroxyhexanoic acid. 1H NMR (CDCl3, 500 MHz) δ 1.44 (m, 2H), 1.60 (m, 2H), 1.68 (m, 2H), 2.37 (t, J=7.5 Hz, 2H), 3.66 (t, J=6.5 Hz, 2H), 5.80 (br, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08388860B2uspto-grants-2013_03