Quote: Originally posted by DraconicAcid | Quote: Originally posted by SplendidAcylation |
Interesting, I have made tin tetrachloride which had no appreciable smell although I tried to avoid inhaling the vapour, would be fun to make some
organotin compounds, maybe via a Grignard reaction. |
The easiest organotin compound to make is tribenzyltin chloride. Reflux tin powder with benzyl chloride. Depending on what solvent you use, you can
get tribenzyltin chloride or dibenzyltin dichloride. |
I made this recently, actually, following the prep in this lab manual:
https://people.uleth.ca/~p.hayes/Chem%203830%20Web%20Page%20...
No particular smell, and I don't think it's particularly toxic. It's not very soluble in ethyl acetate, so the extraction left most of the product
behind.
I'm trying to figure out how do deal with the waste (which probably contains benzyl bromide and various organotin crap) and how to get the damned
white stains off the glassware.
Nice! This is definitely going on my to do list!
Do you know any of the properties of it, is it highly toxic like some other organotin compounds? |