HRID461030
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
Following essentially the same procedure described in Example 7 above and substituting 4-(α-aminoethyl)-1,1-dimethyl-6-tert.-butylindane for the α-methyl-p-phenethylbenzylamine hydrochloride above, results in the formation of 2-[1-(6-tert.-butyl-1,1-dimethyl-4-indanyl)-ethylimino]hexahydro-1H-azepine hydrochloride, having a M.P. of 257°-8° C. (dec.).