Author Topic: 4-Fluoroamphetamine: A full report.  (Read 16544 times)

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grandpa

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but the light-yellow solution did not crystallize
« Reply #20 on: July 09, 2004, 08:14:00 AM »
Well

According to Post 422844 (Bandil: "Verification of Bariums research", Methods Discourse), everything should be fine. Ratios are all in line with what Bandil wrote.

BUT:

the light-yellow solution did not crystallize ... so additional water was added ... Another 4.26 mL of nitroethane (8.46 mmol) was added, followed by 0.25 mL of n-butylamine

Meaning that for this very specific aldehyde the catalyst (methylamine) FAILED to complete the reaction...

WHY ????

Bandil

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Activation
« Reply #21 on: July 09, 2004, 09:39:00 AM »
grandpa>

In my post

Post 422844

(Bandil: "Verification of Bariums research", Methods Discourse)
, 2,5-dimethoxybenzaldehyde was used as the substrate. This is highly activate compared to 4-fluorobenzaldehyde, and gives much higher yields in the condensation reactions. That is most likely the reason that methylamine failed with 4-fluorobenzaldehyde.

Generally speaking its a good idea to use a N-alkylamine (-propyl or -butyl) in a small excess of GAA (compared to the catalst) for the condensation, if you are working with the not so activated substrates.

Kind regards
Bandil