Reaktion #54545
ord-2b7431e995a74a5fb28e43785fa3f5f3
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1workup.DISSOLUTIONdissolves
- 2Temperaturis then heated for two hours at 95°
- 3TemperaturThe reaction solution is cooled
- 4Filtrationfiltered
- 5Sonstigeevaporated in vacuo
- 6Sonstigeto give an oil
- 7Waschenwashed with aqueous sodium bicarbonate solution
- 8TrocknenThe organic phase is dried (MgSO4)
- 9Sonstigeevaporated to an oil
- 10workup.ADDITIONtreated with HCl in isoproanol
- 11SonstigeThe resulting crude solid is removed by filtration
- 12Sonstigerecrystallized from acetonitrile-ether
Vorschrift
A solution of 45 g. (0.3 moles) of 1-[2-(dimethylamino)-ethyl]-1,4-cyclohexadiene from Example 3(a) in 1.5 l. of dry glacial acetic acid is treated with 100 g. of silver acetate and 75 g. of iodine. The mixture is stirred until most of the iodine dissolves and is then heated for two hours at 95°. The reaction solution is cooled, filtered and evaporated in vacuo to give an oil. The oil is taken up in ethyl acetate and washed with aqueous sodium bicarbonate solution. The organic phase is dried (MgSO4) and evaporated to an oil. The oil is taken up in ethyl acetate and treated with HCl in isoproanol. The resulting crude solid is removed by filtration and recrystallized from acetonitrile-ether to yield dl-trans-4-[2-(dimethylamino)-ethyl]-4-cyclohexene-1,2-diol, diacetate ester, hydrochloride salt.