El_Zorro
(Hive Addict) 01-03-03 09:53 No 395069 |
solvent inert to CaC2? | Bookmark | ||||||
What solvents are inert towards CaC2? More specifically, one that acetamide would be fairly soluble in. It is seductive, way too seductive. -Eleusis |
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pHarmacist (Hive Addict) 01-03-03 09:55 No 395070 |
What? | Bookmark | ||||||
What does this has to do with: Novel synthetic routes to psychoactive materials "Turn on, Tune in and Drop Out" |
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El_Zorro (Hive Addict) 01-03-03 10:14 No 395075 |
Well, I didn't really mention it in the ... | Bookmark | ||||||
Well, I didn't really mention it in the question but I was asking this so that I could start forming a procedure for dehydrating acetamide to acetonitrile. So if anybody has thoughts on that too, I'd like to hear them. It is seductive, way too seductive. -Eleusis |
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Rhodium (Chief Bee) 01-03-03 10:45 No 395088 |
Solvents compatible with calcium carbide | Bookmark | ||||||
You want a solvent not containing any acidic hydrogens or other functional groups sensitive to bases. Such solvents include hydrocarbons (like hexane/toluene) and ethers (THF/Et2O). Chlorinated hydrocarbons (DCM, chloroform) might react, so don't use them just to be safe. Esters, alcohols and ketones and any solvents not properly dried are directly unsuitable. |
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Tengo (Newbee) 01-03-03 18:07 No 395154 |
Would CaC2 dissolve in benzaldehyde, forming... | Bookmark | ||||||
Would CaC2 dissolve in benzaldehyde, forming (after acidification) 1,4-diphenyl-1,4-dihydroxy-2-butyne? CaC2 + 2Ph-CHO -> Ph-C(OH)-C---C-C(OH)-Ph |
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Rhodium (Chief Bee) 01-03-03 18:43 No 395160 |
According to what mechanism? | Bookmark | ||||||
According to what mechanism? |
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Tengo (Newbee) 01-03-03 19:56 No 395173 |
Just a thought... C 2 2- being such a strong... | Bookmark | ||||||
Just a thought... C22- being such a strong base, that it would add to the carbonyl and making a hydroxy... SN2 basically... Well... a nucleophile attack anyway... If CaC2 won't dissolve in benzaldehyde, then this wouldn't work. But perhaps with another solvent...? |
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Tengo (Newbee) 01-12-03 05:24 No 397396 |
Anybody...any knowledge about this...? | Bookmark | ||||||
Anybody...any knowledge about this...? |
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PolytheneSam (Master Searcher) 01-12-03 16:44 No 397550 |
Maybe you could heat acetamide and CaC2 ... | Bookmark | ||||||
Maybe you could heat acetamide and CaC2 together without a solvent. Try a small amount in a test tube. You could connect a one hole rubber stopper and 90 degree piece of glass tubing to the test tube and then connect a condenser to it and see if you can distill off any CH3CN. http://www.geocities.com/dritte123/PSPF. The hardest thing to explain is the obvious |
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