1-Phenyl-2-nitropropene (P2NP) Video Synthesis From Benzaldehyde and Nitroethane. Henry Reaction.

ASheSChem

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i have tried ! and it's my actual yield record haha thanks !!

55gr benzaldehyde
40gr nitroethane
10ml acid acetic 80°
3ml isopropanol 99.9%
10ml cyclohexylamine

2:20 p.m. - start of mixing, hotplate at maximum
2:28 p.m. - seems homogeneous to me, with small oily reflections but if I don't see any bubbles
2:32 p.m. - I see bubbles forming in the liquid
2:33 p.m. - I lower the temperature (as I usually do) and turn on the mixer, strong for a few minutes then reduce it a little
6:00 p.m. - I stop and let it cool
7:00 p.m. - add 100ml of isopropanol, mix well (magnetic) and freeze.

09:00 a.m. - I start to filter by gravity the frozen product by mixing regularly
12:00 p.m. - transfer to a pyrex dish for the end of drying (in an incubator)
8:30 p.m. - weighed and transferred to the fridge, 67.7gr. - (71.11%)

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flyhigh

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with same quantities can you suggest what quantity of n-butlyamine to be used ? instead of cyclohexylamine ?
 

flyhigh

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is it 55grams benzaldehyde or 55ml ? coz density is 1.04gm/L and in the picture your flask size is 200ml , so im guessing it must be 55ml
please suggest
 

ACAB

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After I have successfully carried out the synthesis as it was shown in the first video, I now have the final question:
What remains besides the product? How can I recycle it?
My mother liquor has two layers, a heavier dark red oily layer and an upper light yellow layer, I assume an IPA/water mixture, from which I could distill the IPA.
Is the lower dark red layer also still usable? Or just waste?
 

UWe9o12jkied91d

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Sounds like you have nitro left, mother liquid should be monophasic and if already red it is more than likely spent.You could add ipa to homogenize everything and toss in freezer
 
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ACAB

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Any advise? I would hate to dump everything into the environment and keep waste to a minimum.
 

UWe9o12jkied91d

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about disposal? if you are in germany or austria you can take in chemical waste no questions asked for free.
Waste solvents can also be dilstilled for reuse, check the thread.
 

Xiao hua

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Please tell me if it is cyclohexene or cyclohexamine? P2np synthesis video. Thanks 😊
 

UWe9o12jkied91d

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cyclohexene is not an amine
 
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Xiao hua

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What is used in this video? Cyclohexene or cyclohaxamine
 

Xiao hua

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what chemical are instead of cyclohaxamine. cyclohaxamine is to get hard from my country. Asian
 

oneimone

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Hi mates. i just need to make me sure that i can use any isomer of butylamine? I dont understand what means that small "n" before bunh2. Of course bunh2 and butanol is restricted in my country so i got to do it on my own. In UK once avaible to buy legal source of butanol is 2-butoxyethanol which i wanted brake with HCl and separate via distilation and later follow google patent to make bunh2, but im not sure i can use butan-2-ol. it is any difference between location OH group ?
 

wael gano

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I tried the synthesis and I ended up with this solution. What is wrong with this? What do I do?
 

wael gano

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8HoqWdtJun
 

UWe9o12jkied91d

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Can you describe procedure you did? Catalyst used, what stirring , what heating, reaction time etc.
Looks to me you got some product and the rest remained unreacted, but its just guess
 

wael gano

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I tried the synthesis and I ended up with this solution. What is wrong with this? What do I do?
7.5 ml of benzaldehyde
6 ml of nitro ethane
3 ml of glacial acetic acid
1.8ml cyclohexylamine
Heating for 3,5 hours
What is wrong with the product of the reaction, something like the unreacted amine?
 

wael gano

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I tried synthesis and ended up with this solution. What's wrong with this? What should I do?
YAnWu1hp7c
 

wael gano

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I tried the synthesis and I ended up with this solution. What is wrong with this? What do I do?
7.5 ml of benzaldehyde
6 ml of nitro ethane
3 ml of glacial acetic acid
1.8ml cyclohexylamine
Heating for 3,5 hours
What is wrong with the product of the reaction, something like the unreacted amine?
Vw7yBtup34
 

UWe9o12jkied91d

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oof, now I read carefully...you should use equal volumes of nitro benzo, that in your picture is unreacted benzaldehyde ofcourse
 
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flyhigh

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youre right its a equimolar ratio of both but considering densities of benzaldehyde and nitroethane calculate the values of both appropriately
 

777m

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So what do you think the real rates should be?
 

flyhigh

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how did you come up with those ratios ? those dont sound so stoichiometric to me.
 
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