John paul III
Hazard to Others
Posts: 110
Registered: 28-4-2018
Member Is Offline
Mood: No Mood
|
|
oxalic acid -> ethylene glycol
Hi guys
An idea came to me: since oxalic acid can be made from ethylene glycol with HNO3/H2SO4, maybe we can make ethylene glycol from oxalic acid? Oxalic
acid can be made by easier route(s), so this could be a nice alt source of EG. I hope you have suggestions!
[Edited on 1-5-2018 by John paul III]
|
|
|
DraconicAcid
International Hazard
Posts: 4333
Registered: 1-2-2013
Location: The tiniest college campus ever....
Member Is Offline
Mood: Semi-victorious.
|
|
Reduction of carboxylic acids, IIRC, requires things like lithium aluminum hydride. So, probably not.
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
|
|
|
Chemi Pharma
Hazard to Others
Posts: 349
Registered: 5-5-2016
Location: Latin America
Member Is Offline
Mood: Quarantined
|
|
The only way I know to reduce acids to alcohols is using LiAlH4 or NaBH4 with metal salts catalist ligands like Ni+2, Cu+2, Zn+2 or Co+2.
But tell me a good reason to spend my money using this expensive reagents to do the reaction you sugested, if Ethylene Glycol is a so dirty cheap and
easy reagent to buy all over the world, even at a gas station or at supermarkets?
|
|
|
Texium
|
Thread Moved
1-5-2018 at 19:14 |
![[*]](images/xpblue/default_icon.gif){kind=icon}
