Abstract

With triallylboron fi-cyc!ocitral gives l-(2,6,6-trimethylcyclohex-l-enyl)but-3-en-l-yl borate, the saponific~t~ion of which yields l-(2,6,6-trimethylcyelohex-l-enyl)but-3-en-l-ol, bp 91-93~ (3 ram), nD 20 1.4950. n-Tributylboron adds to methyl vinyl ketone in the 1,4 position with the formation of oct-2-en-2-yl di-n-butylborinate (V) with bp I00-I03~ (1.5 mm); nD 2~ 1o4300o Found%: C 76.06; H 13.15; B 4.57. CI6H23BOo Calculated%: C 76.13; H 13.18; B 4.36~ The hydrolysis of (V) gives n-hexyl methyl ketone.

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