Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: Producing Anthracene from Napthalene? possible?
Matsumoto_Hideki
Banned





Posts: 103
Registered: 27-12-2004
Member Is Offline

Mood: detonated

mad.gif posted on 8-1-2005 at 15:09
Producing Anthracene from Napthalene? possible?


Hey I am looking to make an organic scintillator from Anthracene using a blue spectra high sensitivity wide area Photodiode. Anyone tell me how to make anthracene?

C10H8 +___?___ = C14H10
View user's profile Visit user's homepage View All Posts By User
Dodoman
Hazard to Self
**




Posts: 79
Registered: 2-8-2004
Member Is Offline

Mood: No Mood

[*] posted on 8-1-2005 at 15:17


I don't quite understand your question but anthracene can be prepared from naphthalene. There is a method called Hawardth synthesis but it's very complecated and I don't know of any other direct method.
View user's profile View All Posts By User
Matsumoto_Hideki
Banned





Posts: 103
Registered: 27-12-2004
Member Is Offline

Mood: detonated

shocked.gif posted on 8-1-2005 at 15:21
Question is simple


ok, good So now that i know it is possible.. this is looking good. thanx
i am wanting to make an organic scintillator and I can't find Anthracene anywere so i will make it instead.
View user's profile Visit user's homepage View All Posts By User
guaguanco
Hazard to Others
***




Posts: 216
Registered: 26-11-2003
Member Is Offline

Mood: heterocyclic

[*] posted on 10-1-2005 at 13:51


Quote:
Originally posted by Dodoman
I don't quite understand your question but anthracene can be prepared from naphthalene. There is a method called Hawardth synthesis but it's very complecated and I don't know of any other direct method.


If you are referring to the Haworth reaction, it looks like it produces phenanthrenes, not anthracenes:

http://themerckindex.cambridgesoft.com/TheMerckIndex/NameReactions/onr176.htm
View user's profile View All Posts By User
Dodoman
Hazard to Self
**




Posts: 79
Registered: 2-8-2004
Member Is Offline

Mood: No Mood

[*] posted on 10-1-2005 at 15:29


Oh sorry about that I got confused between phenanthrene and anthracene.

But you can prepare phthalic anhydride from naphthalene via V2O5 and O2.
View user's profile View All Posts By User
Marvin
National Hazard
****




Posts: 995
Registered: 13-10-2002
Member Is Offline

Mood: No Mood

[*] posted on 10-1-2005 at 22:27


Also napthalene, so I see no problems with an anthracene version.

http://www.chem.ed.ac.uk/teaching/undergrad/chemistry2/lectu...

There is an anthracene version of Haworth listed by google but its registered users only. I'd be guessing it works like dodoman thinks. Benzene + pthallic anhydride.

Pthallic acid can also be made by permanganate oxidation of napthalene and then dehydrated. Might be easier than vapour phase oxidation.

There are other methods to anthracene I can think of but they go via benzyl chloride, chiefly as byproducts of biphenyl synthesis and I'm not sure how well this could be adapted.
View user's profile View All Posts By User

  Go To Top