Reacción #2314291
ord-052919a58443459794b1083aada7652c
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroTo a round-bottom flask equipped with a stirbar
- 2Extracciónextracted with 1:1 hexanes
- 3LavadoThe combined organic layers are washed with brine
- 4Secadodried over potassium carbonate
- 5Concentraciónthe solution is concentrated in vacuo
- 6FiltraciónFiltration through silica gel using 10% ethyl acetate in hexanes
- 7Otrogives the pure product
Procedimiento
To a round-bottom flask equipped with a stirbar is added phenol 3H (R=pentyl) (5 g), (4-(4-Methyl-3-pentenyl)-1-cyclohexenyl)carboxylic acid (R=n-pentyl) (3.3 g), dicyclohexylcarbodiimide (5.11 g), dimethylaminopyridine (202 mg), and anhydrous tetrahydrofuran (50 mL). The reaction is stirred overnight, at which time the solution is poured into water and extracted with 1:1 hexanes:ethyl acetate. The combined organic layers are washed with brine and dried over potassium carbonate, and the solution is concentrated in vacuo. Filtration through silica gel using 10% ethyl acetate in hexanes gives the pure product.