反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of 0.28 g. of 1-(p-chloro-α,α,α-trifluoro-m-tolyl)cyclopropanedicarboximide in 10 ml. of benzene is added one ml. of Vitride®. This is refluxed for one hour, cooled to ambient temperature, and the excess hydride reagent is decomposed with one ml. of 10 N sodium hydroxide. The benzene layer is washed with water, dried over magnesium sulfate and evaporated under reduced pressure to give an amber-colored oil. This is dissolved in ether and dry hydrogen chloride is bubbled into the solution. The resultant precipitate is collected by filtration and recrystallized from isopropyl alcohol to give 1-(p-chloro-α,α,α-trifluoro-m-tolyl)-3-azabicyclo[3.1.0]hexane hydrochloride. Purification of the hydrochloride by recrystallization from acetonitrile gives colorless crystals, m.p. 164°-166° C.
WORKUP
后处理
- temperatureThis is refluxed for one hour
- washThe benzene layer is washed with water
- dry with materialdried over magnesium sulfate
- customevaporated under reduced pressure
- customto give an amber-colored oil
- customdry hydrogen chloride is bubbled into the solution
- filtrationThe resultant precipitate is collected by filtration
- customrecrystallized from isopropyl alcohol