Would 1,4-dichlorobenzene be a possibility, too? I see it is one of the ingredients in urinal cakes, it's less toxic & flammable, though it
apparently sublimes a bit at room temperature.
I'm supposing dechlorination to benzene could also be done via NaOH, correct? Would a substitution reaction be more direct/easier since it's phenol,
not benzene I'm after?
I don't have my reference library available (I am on holiday, after all), however a little bit of poking around on wikipedia suggests that urinal
blocks are now para-dichlorobenzene-free, though no citation is given. I note that Recochem (parent of Diggers) sells the stuff in flake and block
form in Australia, so it doesn't appear to have been banned or restricted. Has anyone purchased from them? It's in their industrial chemicals
division, but a cursory search through recochem.com.au failed to yield their business terms.
[Edited on 2-1-2013 by Gearhead_Shem_Tov]
[Edited on 2-1-2013 by Gearhead_Shem_Tov][/]
The dichloro is in some moth balls, if I'm not mistaken. Diggers/Recochem are stocked wildly in oz retail, they list phenyle as the active ingredient
in their wheelie bin sanitizer. I'm not sure but expect its a Creosol/Phenol/Xylenol mixture.
Hydrolysis of chlorobenzene by steam or base would yield phenol. I'm not sure the dichloro would be suitable feed stock for phenol, at least directly.
Where there is a will there is a way though. If I were in the same possition as you, I would be saving the opportunity to obtain the neigh on
impossible or the ridiculously expensive items comparative to the ease and availability of what is locally synthesized &/or obtainable.
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