Reacción #524264

ord-3e4b6eb975ea4982a5ab2c1e96a3f3a8

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

Sym. octahydroacridine was prepared by converting cyclohexanone to di-(2-oxo-cyclohex-1-yl)-methane and further reacting with hydroxylamine according to the method of Gill et al (JACS 1952, 74, 4923) and was isolated as a colourless oil b.p. 110°-15°/0.5 mm. in 40% overall yield.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04029668uspto-grants-1977_06