Chemical Forums
Specialty Chemistry Forums => Materials and Nanochemistry forum => Topic started by: Rosalind Franklin on May 22, 2019, 01:02:46 AM
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Hey guys!
I am trying to use ZnO nanoparticles(ZnO NPs) as catalyst for Coumarin synthesis. I tried Knoevenagel condensation under thermal conditions. I went with the literature and added salicylaldehyde, diethylmalonate and ZnO NPs but I am not getting any solid product. From what I know about Knoevenagel condensation, it requires a mild base which can abstract the acidic proton from diethylmalonate. Could lack of mild base be the reason for not getting any product?
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I have not had recreating luck with those transition metal NP papers. I gave iron NPs a shot to do NO2 reduction and got classic glop. I think these reactions are quite sensitive to NP size, surface chemistry, etc.
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I have not had recreating luck with those transition metal NP papers. I gave iron NPs a shot to do NO2 reduction and got classic glop. I think these reactions are quite sensitive to NP size, surface chemistry, etc.
Yes, I got some glop too! I tried using piperidine as my base and had no luck yesterday. I read somewhere that an excess of piperidine can make the product gooey. So, today I reduced the amount of piperidine and it worked! TLC looks good but I need to characterise further. Thanks a lot!
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Awesome to hear your success story!
Care to share the paper you were following?
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Yeah sure! This is the paper I referred to.
https://www.ias.ac.in/article/fulltext/jcsc/123/05/0615-0621 (https://www.ias.ac.in/article/fulltext/jcsc/123/05/0615-0621)
I also referred to a lab report on the synthesis of 3-Carbethoxycoumarin. Not a published work but I found it useful.
http://sites.psu.edu/timikeyi/wp-content/uploads/sites/10213/2014/02/Synthesis-of-3-Carbethoxycoumarin.docx (http://sites.psu.edu/timikeyi/wp-content/uploads/sites/10213/2014/02/Synthesis-of-3-Carbethoxycoumarin.docx)