The
aliphatic-acid-mediated dehydration of C6–10-α,ω-alkanediols
to alkadienes proceeds in a stepwise
manner: C6–10-α,ω-alkanediols react
with aliphatic acids first to generate diesters; subsequent pyrolysis
of the latter produces alkadienes. The highest yields of 1,5-hexadiene,
1,7-octadiene, and 1,9-decadiene were up to 70.3, 74.8, and 90.3%,
respectively. It turned out that pyrolysis favors the diester with
a longer carbon chain more, while acetic acid outperformed the other
aliphatic acids in the pyrolysis step that a relatively lower temperature
was enough for a high yield of alkadienes.