- Synthesis of diketones and ω-hydroxy ketones from methyl ketones and α,ω-diols by an [IrCl(eod)]2/PPh3/KOH system
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ω-Hydroxy ketones and diketones, which are important starting materials for the synthesis of cycloalkanones and heterocyclic compounds, were prepared by the one-step reaction of methyl ketones with α,ω-diols under the influence of an iridium complex and a base. The selectivity of ω-hydroxy ketones and diketones could be controlled by varying the starting ratio of methyl ketones to α,ωdiols. For example, reaction using acetophenone (5 equiv) with respect to 1,6-hexanediol (1 equiv) in the presence of [IrCl(cod)]2, PPh3, and KOH without solvent gave 1,10-diphenyl-1,10-decane-dione in almost quantitative yield, while reaction using acetophenone (1 equiv) to 1,6-hexanediol (4 equiv) led to 8-hy-droxy-l-phenyl-l-octanone in 92% yield. This methodology was successfully extended to the reaction of arylacetonitriles with α.ω-odiols leading to diaryldinitriles.
- Maeda, Kensaku,Obora, Yasushi,Sakaguchi, Satoshi,Ishii, Yasutaka
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experimental part
p. 689 - 696
(2009/04/07)
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- Effects of methylene chains on photoreactions of diphenylalkanediones and phenylalkenones
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Upon conventional UV-irradiation of I,ω-diphenylalkane-1,ω-dione (PhC(O)-(CH2)n-C(O)Ph, n= 5, 6, 7, 8, and 10) in acetonitrile using a medium-pressure Hg lamp, an intramolecular γ-hydrogen abstraction of the triplet ketone (type II p
- Nakamura, Mitsunobu,Miki, Masamichi,Majima, Tetsuro
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p. 415 - 420
(2007/10/03)
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