Process for the production of 2,2,6,6-tetraalkyl-4-piperidylamin

Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...

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546189, 546191, 546223, 546244, C07D40112, C07D40114

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active

046071040

ABSTRACT:
2,2,6,6-tetraalkyl-4-piperidylamines are produced by reacting an amine with a 2,2,6,6-tetraalkyl-4-piperidone in the presence of a catalyst selected from the group consisting of platinum, nickel and cobalt, employing a reaction medium comprising (a) between about 10 and 100 weight percent water and (b) between 0 and about 90 weight percent of a polar organic compound selected from the group consisting of C.sub.1 -C.sub.10 aliphatic alcohols and C.sub.2 -C.sub.6 aliphatic glycols.

REFERENCES:
patent: 4104248 (1978-08-01), Cantatore
patent: 4326063 (1982-04-01), Son
patent: 4415688 (1983-11-01), Minagawa et al.
P. N. Rylander, Catalytic Hydrogenation Over Platinum Metals, pp. 12-13, Academic Press (1967).
P. N. Rylander, Catalytic Hydrogenation in Organic Syntheses, pp. 3-4, Academic Press (1979).
M. Freifelder, Catalytic Hydrogenation in Organic Synthesis Procedures and Commentary, p. 3, Wiley and Sons.
M. Freifelder, Practical Catalytic Hydrogenation, pp. 81-82, Wiley and Sons.

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