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100045-83-8
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tributyl((methoxymethoxy)methyl)stannane
???(??):
SKL977;(MethoxyMethoxyMethyl)tributyltin;TRIBUTYL(METHOXYMETHOXYMETHYL)STANNANE;[(Methoxymethoxy)methyl]tributylstannane;Tributyl[(methoxymethoxy)methyl]stannane AldrichCPR
CBNumber:
CB0384872
???:
C15H34O2Sn
??? ??:
365.14
MOL ??:
100045-83-8.mol
MSDS ??:
SDS

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?? ?
84-87 °C(Press: 0.05 Torr)
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soluble in Chloroform, Dichloromethane, Ethyl Acetate, Methanol
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  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? T,N
?? ???? ?? 21-25-36/38-48/23/25-50/53
????? 36/37/39-45-60-61
????(UN No.) UN 3146 6.1 / PGII
WGK ?? 3
????(GHS): GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
?? ?: Danger
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H301 ??? ??? ?? ?? ?? - ?? ?? 3 ?? GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
H312 ??? ???? ??? ?? ?? ?? - ?? ?? 4 ?? GHS hazard pictograms P280,P302+P352, P312, P322, P363,P501
H315 ??? ??? ??? ????? ?? ????? ?? 2 ?? GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 2A ?? GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H372 ??? ?? ?? ???? ??(??, ??? ?? ??? ?? ??? ??)? ??? ??? ?? ???? ?? - ?? ?? ?? 1 ?? GHS hazard pictograms P260, P264, P270, P314, P501
H410 ??? ??? ?? ????? ?? ??? ?? ????? ?? - ?? ?? 1 ?? GHS hazard pictograms P273, P391, P501
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P202 ?? ?? ?? ??? ?? ???? ??? ???? ???.
P273 ???? ???? ???.
P280 ????/???/???/?????? ?????.
P301+P310 ???? ?? ????(??)? ??? ????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.

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Colourless Liquid

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Tributyl((methoxymethoxy)methyl)stannane is a reagent used to conduct (Methoxymethoxy)methyl additions.

Synthesis

The Preparative Method of tributyl((methoxymethoxy)methyl)stannane: The most convenient preparation involves the two-step procedure outlined in eq 1. The first step involves the addition of Tri-n-butylstannyllithium to Paraformaldehyde, as Still described. In the second step, methoxymethylation is achieved via acetal exchange with Dimethoxymethane, promoted by Boron Trifluoride Etherate and Molecular Sieves. This procedure provides the desired reagent in higher yields compared to an alternative procedure which uses Phosphorus(V) Oxide to promote the acetal exchange step. This method is also superior to an alternative approach, which involves alkylation of (tributylstannyl)methanol with Chloromethyl Methyl Ether.
tributyl((methoxymethoxy)methyl)stannane

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