Cyclohexanone → N-cyclohexylidene-(2-methylpropenylamine)

Participants

Reaction Steps

The procedure described in Example (1a) is repeated, except that 302.5 g (2 mols) of N-cyclohexylidene-(2-methypropenylamine) and 250 g (4.62 mols) of 1,3-butadiene are used. Distillation yields 382 g (1.48 mols) of 3,3-dimethyl-12,12-pentamethylene-1-aza-1,5,9-cyclododecatriene; boiling point 96° C./4 Pa; nD20 =1.5116. The N-cyclohexylidene-(2-methylpropenylamine) was prepared from cyclohexanone and methallylamine, with subsequent isomerisation of the reaction product with potassium tert.-butylate; boiling point 96° C./1,700 Pa; nD20 =1.5160.

Provenance & Evidence