Reacción #346449
ord-1f4109b6444941dcb8d0392730d445b1
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otroformed by the addition of 50 mg
- 2OtroAfter approximately 4 hours the solvent is removed from the reaction mixture and 20 ml
- 3workup.ADDITIONof water is added to the residue
- 4ExtracciónThe resultant aqueous mixture is extracted with ether
- 5Lavadothe ether extracts washed with water
- 6Secadodried over magnesium sulfate
- 7Otroevaporated
Procedimiento
2,3-Epoxypropyl isopropyl ether (1.16 g.) in several ml. of dry tetrahydrofuran is added to a stirred suspension formed by the addition of 50 mg. of sodium hydride (56% dispersion in mineral oil) to 2.2 g. 8. of n-dodecylthiol in 50 ml. tetrahydrofuran. The mixture is then stirred at 60° C. After approximately 4 hours the solvent is removed from the reaction mixture and 20 ml. of water is added to the residue. The resultant aqueous mixture is extracted with ether and the ether extracts washed with water, dried over magnesium sulfate and evaporated to yield 1-(n-dodecylthio)-3-isopropoxy-2-propanol.