Reacción #95527
ord-e5f165f41b8a43c881a56271e218a452
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otrodid not exceed 10° C
- 2ExtracciónThe product was extracted with ether
- 3Lavadothe ethereal solution washed
- 4Secadodried with sodium sulphate
- 5Otroevaporated
- 6Otroto give an oil which
- 7OtroThe solid was recrystallised from a mixture of benzene and light petroleum
Procedimiento
To a cooled solution of 2-hydroxy-2,3-dihydro-3,3-dimethylbenzofuran-5-yl methanesulphonate (8.0 parts) in dry pyridine (42 parts) was added benzoyl chloride (4.75 parts) at such a rate that the temperature did not exceed 10° C. After one hour the mixture was poured into a slight excess of dilute hydrochloric acid. The product was extracted with ether and the ethereal solution washed, dried with sodium sulphate and evaporated to give an oil which solidified on scratching. The solid was recrystallised from a mixture of benzene and light petroleum to give 2-benzoyloxy-2,3-dihydro-3,3-dimethylbenzofuran-5-yl methanesulphonate (5.1 parts), melting point 102°-104° C.