1959
DOI: 10.1021/jo01091a626
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Notes: Reactions of Zirconium Tetrachloride with Acetone

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“…Aldehydes and ketones are alcohols when in their enol forms, and show a tendency to form alkoxides. Thus, trichlorozirconiumisopropenoxide was isolated as a reaction product of zirconium tetrachloride with acetone: ZrCl4 + CH3COCH3-* Cl3ZrOC : CH2CH3 + HC1 A similar reaction occurred between zirconium tetrachloride and methylisopropyd ketone (21). Substitution products in which there was replacement of more than one chlorine were not obtained, apparently due to a catalytic effect of zirconium whereby condensation of the ligands occurred with liberation of water and hydrolysis of the alkoxide.…”
Section: Ketonates and Carboxylatesmentioning
confidence: 96%
“…Aldehydes and ketones are alcohols when in their enol forms, and show a tendency to form alkoxides. Thus, trichlorozirconiumisopropenoxide was isolated as a reaction product of zirconium tetrachloride with acetone: ZrCl4 + CH3COCH3-* Cl3ZrOC : CH2CH3 + HC1 A similar reaction occurred between zirconium tetrachloride and methylisopropyd ketone (21). Substitution products in which there was replacement of more than one chlorine were not obtained, apparently due to a catalytic effect of zirconium whereby condensation of the ligands occurred with liberation of water and hydrolysis of the alkoxide.…”
Section: Ketonates and Carboxylatesmentioning
confidence: 96%