1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine → 1-(Cyclooct-2-enyloxy)-2,2,6,6-tetramethyl-4-hydroxypiperidine

Beteiligte Stoffe

Reaktionsbedingungen

Reaktionsschritte

A mixture of 15.0 g (0.09 mol) of 1-oxyl-4-hydroxy-2,2,6,6-tetramethylpiperidine and 126.6 g (1.15 mol) of cyclooctene is heated under a nitrogen atmosphere at 87-88° C. for 40 hours. The reaction mixture is filtered to remove 1,4-dihydroxy-2,2,6,6-tetramethylpiperidine, and the filtrate is washed with 5% ascorbic acid (2×50 mL) and distilled water (2×50 mL). The organic phase is dried over anhydrous magnesium sulfate and the volatiles removed in vacuo. The residue is crystallized from heptane to give 4.40 g (36% yield) of the title compound as a white solid.

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