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YT2095

Ester Experiments :)

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Re KMnO4 and methanol-

"just mix the two' date=' maybe heat a little. i dont think heat is required. you'll end up with a precipitate. just gravity filter"

I don't think that's a good idea. Mixing solutions of the 2 in water is a safer bet.[/quote']

In my experience, mixing [math]KMnO_{4}[/math] and methylated spirits will cause the mixture to ignite.

 

Does anyone know how dimethyl methylphosphonate is produced industrially (I think mostly as a flame retardant)?

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Just a note - instead of using the [math][/math] tags for your chemical equations, you can just use [ce][/ce]

 

i.e.

[ce]KMnO4[/ce]

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Would it be easier with phosphorous acid ([math]H_{3}PO_{3}[/math'])?

I think the proper term is phosphonic acid ([ce]HP(O)(OH)2[/ce]), phosphorous acid being the tautomer [ce]P(OH)3[/ce].

:embarass:

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my Latest is trying to make Phenyl Oxalate ester.

sadly I have no Phenol :(

the closest I have is Catechol and Hydroquinone.

 

after that, p-Dichlorobenzene, Methyl benzene, Benzoic acid and Trinitro Phenol. and I think almost every chemist has pure ASA in a jar too.

 

anyone have any ideas how I might be able to pull this off using these precursors for the Phenol side?

 

I have the Oxalic acid and all the other things likely to be required.

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Phenol can be made by decarboxylation of salicylic acid (derived from ASA of course) with NaOH or Ca(OH)2 in a manner that is analagous to the decarboxylation of benzoic acid to yield benzene.

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my Latest is trying to make Phenyl Oxalate ester.

sadly I have no Phenol :(

the closest I have is Catechol and Hydroquinone.

 

after that, p-Dichlorobenzene, Methyl benzene, Benzoic acid and Trinitro Phenol. and I think almost every chemist has pure ASA in a jar too.

 

anyone have any ideas how I might be able to pull this off using these precursors for the Phenol side?

 

I have the Oxalic acid and all the other things likely to be required.

 

Making some glow sticks are you yt? (if your not and that made me sound like an idiot it glows when you add h2o2)

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Wow, okay, the last post was in 2007. I hope someone sees this. I'm doing a science fair (mandatory) project, and esterification looks interesting. Please reply if anyone sees this, because I'd like some help. Thanks!

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When you submit a new post, it bumps that discussion thread to the top of the forum in which it resides, and also presents it on the "Today's Posts" search which many members use. In short, people will see this. Go ahead and ask your specific questions, and if someone knows the answers, they will share them with you. Good luck on the project, and welcome to SFN. :)

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