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All 2 posts | Subject: Nitroethane via Et3N or what??? | Please login to post | Down | |||||
lutesium (Stranger) 07-19-04 19:25 No 520316 |
Nitroethane via Et3N or what??? | |||||||
Hi For almost A YEAR swim is looking for an attractive way to make nitroethane that will rush you to the lab immediately to experiment. But he has no luck :( He has an idea. He wants to get to the holy molecule through triethylamine. Is it possible to ozidatively cleveage that Et3N to EtNO2 via a strong oxidizer? And once he read somewhere on this site that EtNO2 can be made via HEtSO4 + NaNO2 not via the good (!) 'ol dry way (OHHH I CAND BEAR IT!!) -by mixing etOH+H2SO4 then distillin w/a NaNO2 sol. and NE distills over w/ steam- but cannnot find that post : ( or is there another way (that you think best) to the sacred little nitro. Thanx ;) |
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lutesium (Stranger) 07-20-04 00:28 No 520358 |
I know that I'm replyn my own thread but ... | |||||||
I know that I'm replyn my own thread but something is bugggin' my mind. Can you use prydine+EtI in acetonitrile as a two phase rxn with nano2 dissolved in H2o and a PTC added? The explanation is to form a quatirnatery ion with prydine and MeI and form a better nucleophile for NO2 which is transferred by the ptc. Are these logical? |
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