dormouse
(Member) 04-22-00 01:48 No 108521 |
dehalogenation of phenolic comps -pambaruka | Bookmark | ||||||
the Hive BB Novel Discourse dehalogenation of phenolic comps profile | register | preferences | faq | search next newest topic | next oldest topic Author Topic: dehalogenation of phenolic comps pambaruka Junior Member posted 10-02-98 09:00 PM ---------------------------------------- can you use formic acid and palladium to reduce trichloro phenol (TCP) to phenol? beagle boy unregistered posted 10-03-98 03:53 PM ---------------------------------------- Very seriously doubt it, but why do you care? Phenol itself is cheap as dirt. What is phenol good for anyway? Besides producing painful blisters and stinking like hell that is. Osmium Member posted 10-05-98 04:51 AM ---------------------------------------- Yes, there are some refs about this sort of dehalogenation, using Pd/C and ammonium formate (?). Don't remember them right now, but I might have a look if you tell me what this might be good for. As beagle said, phenol is not that hard to get to justify its synthesis. drone 342 Member posted 10-07-98 10:41 AM ---------------------------------------- Some phenols are OTC -- hydroquinone, vanillin, etc. If memory serves, I think even phenol itself is available. I'm really curious now. What the hell would someone want phenol for? -drone #342 Contact Us | the Hive Powered by: Ultimate Bulletin Board, Version 5.39a |
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