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Silane disproportionation results in spontaneous ignition Stephen L. Buchwald
Chemical & Engineering News (29 Mar 1993) Vol. 71, No. 13, pp. 2. We have recently reported a catalyst system for the conversion of esters to alcohols that functions in an air atmosphere using a catalytic amount of titanium isopropoxide (Ti[OCH(CH3)2]4) and triethoxysilane (HSi[OCH2CH3]3) as the stoichiometric reductant. In our communication [J. Org. Chem., 57, 3751 (1992)], we warned that, in the absence of substrate and under an inert atmosphere, HSi(OCH2CH3)3 is disproportionated by Ti(OCH(CH3)2)4 to form SiH4, a pyrophoric gas. Such disproportionations, catalyzed by many metal complexes, have been reported in the literature [Adv. Organomet. Chem., 19, 213 (1981); Can. J. Chem., 68, 471 (1990)]. It has come to our attention that silane production may occur with
our catalyst system even in the presence of substrate, especially if
the reaction is run on a large scale or a large excess of silane is
used. A user of the procedure has informed us that he attempted to
perform the reduction of a methyl ester (90 millimoles) using
HSi(OCH2CH3)3(313 millimoles, 3.5 equivalents). He first added the
reagents to the reaction vessel, which was flushed with nitrogen,
and the reaction was vented to an oil bubbler. After heating to 50
At Massachusetts Institute of Technology, we have run this reaction
on scales of up to 50 millimoles, but without event when run under
an atmosphere of dry air, which we surmise may quench any SiH4 as
soon as (or before) it is formed. When the reaction is run under an
inert atmosphere, the SiH4 can build up, especially after the
reduction reaction is complete, leading to fires when the mixture is
finally exposed to air. We strongly urge those who are contemplating
the use of this procedure to be alert to the possibility of SiH4
formation and possible exotherms and to take suitable precautions.
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