|
|
||||||||
|
Natrix (Stranger) 09-24-01 22:44 No 216749 |
|
Cl -> OH | Bookmark | |||||
|
How difficult would it be to make 2-methyl-hydrochinone from 4-chloro-3-methylphenol (PCMC) ? PCMC is a biocide and is used against bacteria, fungi and yeast. [image] |
||||||||
|
|
||||||||
|
PolytheneSam (Master Searcher) 09-24-01 23:12 No 216754 |
|
Re: Cl -> OH | Bookmark | |||||
|
I saw something in a chemistry book about a Dow Chemical process for making phenol from chlorobenzene using NaOH solution at 350 degrees C under pressure. http://www.geocities.com/dritte123/PSPF. |
||||||||
|
|
||||||||
|
Rhodium (Chief Bee) 09-24-01 23:13 No 216755 |
|
Re: Cl -> OH | Bookmark | |||||
|
Reflux in strong sodium hydroxide solution together with copper powder, for at least 24h. A general method is described for 5-hydroxyvanillin in: https://www.rhodium.ws/chemistry/mmda.me If you were planning on using it for 2,5-dimethoxytoluene, I'd suggest you methylate the starting material first, for easier workup, and possibly better yields. |
||||||||
|
|
||||||||
|
Natrix (Stranger) 09-25-01 12:22 No 217030 |
|
Re: Cl -> OH | Bookmark | |||||
|
Thanks for your answers PolytheneSam and Rhodium. Although the yield might be low (US.P. 3,778,481), the substance is very interesting because it is sold otc and it is inexpensive. |
||||||||
|
|
||||||||
|
foxy2 (Distinctive Doe) 09-25-01 17:40 No 217065 |
|
Re: Cl -> OH | Bookmark | |||||
|
If you have access to an ultrs sonic bath I would put the reaction in it periodically. It should increase yeilds Do Your Part To Win The War |
||||||||