Reacción #1197352
ord-b2581a2e87d94f09b65aaaadae7f350e
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.ADDITIONTo the solution was added lithium acetylide ethylenediamine complex (180 mg, 1.95 mmol)
- 2Extracciónthe reaction mixture was extracted with ether
- 3SecadoThe extract was dried over Na2SO4
- 4Otroevaporated in vacuo
- 5Otroto remove the solvent
- 6Otroto give a crude product, which
- 7Otrowas purified with silica gel column chromatography
Procedimiento
A solution of 6,10-dimethyl-11-(2-tetrahydropyranyl) oxy-5,9-undecadien-2-one (90 mg, 0.31 mmol) in tetrahydrofuran (5 ml) was stirred on an ice bath under argon atmosphere. To the solution was added lithium acetylide ethylenediamine complex (180 mg, 1.95 mmol), and the mixture was warmed to room temperature and stirred for 3 hours. After addition of saturated aqueous ammonium chloride (2 ml), the reaction mixture was extracted with ether. The extract was dried over Na2SO4 and evaporated in vacuo to remove the solvent to give a crude product, which was purified with silica gel column chromatography to obtain 3,7,11-trimethyl-12-(2-tetrahydropyranyl)oxy-6,10-dodecadien-1-in-3-ol (75 mg, 75%).