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Stannane, tributyl[1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethenyl]- synthesis

1synthesis methods
(tri-n-butylstannyl)ethanone

52168-13-5
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18162-48-6 Synthesis
tert-Butyldimethylsilyl chloride

18162-48-6
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$9.00/5g

Stannane, tributyl[1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethenyl]-

136201-90-6
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Yield: 63%

Reaction Conditions:

with N,N,N,N,N,N-hexamethylphosphoric triamide;lithium diisopropyl amide in tetrahydrofuranSn-compound added to LDA in THF (stirring, -78°C, under N2); temp. allowed to reach 0°C for 15 min; soln. cooled to -78°C; addn. of chlorotrimethylsilane; mixt. allowed to reach room temp.; HMPA added, quenching with water, extn. (pentane);

References:

Verlhac, Jean-Baptiste;Pereyre, Michel;Shin, HeeAn [Organometallics,1991,vol. 10,# 9,p. 3007 - 3009]