Anthranilic Acid : Organic synthesis

[@WaffleStaffel]

Nice, I was just pondering methyl anthranilate yesterday :) Your final product is the cleanest looking in all the videos I've seen.

[@gayatriarde968]

Crystals formed are really good So satisfying ☺️

[@chemistrylovers742]

Please make a video on the preparation of Hoffman Bromamide synthesis

[@foc2241]

Beautiful crystals :)

[@binalpatel716]

Thank you very much nice explain

[@manjeshkushwaha7594]

Please make a video on ternary mixture separation of organic compounds

[@gayatriarde968]

I loved your video ☺️

[@storytelling_saga]

How to recrystalize it?

[@neeav6407]

thank you sir

[@noodlesoup2281]

Hypobromite must be a much cleaner than hypochlorite! I wanted to ask why it is you think it ended up darker after recrystallisation? Also before acidifying what temperature do you cook it back down to?

[@crystalmik8410]

Are you sure that the fumes are NH4Cl? There is no ammonia used in those steps. I have the same issue and also the feeling this could be hydrazine hydrochloride from contaminated phthalimide

[@petevenuti7355]

How hard would it be to make phthalic acid from PETE plastic bottles? To make the phthalmide from.. (yes I've seen the Nile red vynal gloves extraction)

[@sambiafilms4228]

Hello Sir, thank you very much for this video I learned a lot from you :) but I still have a question, if I would like to use activated charcoal to discolor the solution how would this work? Should it just be added to the solution that is put in the refrigerator? and if yes. how many grams of charcoal per ml of solution? thank you for sharing your Knowledge warm Regards

[@punishedgloyperstormtroope8098]

That should work maybe also try ethanol recrystallisation

[@jhyland87]

Would _nearly_ glacial AcOH be sufficient? Eg: 98% or so? Since theres already some water in the reaction i would assume 98% AcOH would be ok as long as the quantity is adjusted to ensure the right amount - correct? *P.S.* great video! Thanks for uploading.

[@dhruvsureka4830]

We tried this experiment earlier but did not receive any product after heating at ,75-80°c any specific reason for the product not precipitating out ??

[@rabiamehtab]

Any alternative for bromine?

[@vibzzlab]

I've heard hypobromite can be used but it do not give reasonable yield

[@rabiamehtab]

@@vibzzlab thank you for reply 👍

[@MediaSubliminal]

It seems that there is not a solid consensus or definition of what is considered 'concentrated HCl" What is considered concentrated? I would imagine it's not critical to most experiments if HCl is simply to lower ph. I'm just curious. I guess I wonder if 10M is concentrated enough. I would like to avoid the expense of ordering and hazard of purifying further.

[@ambition8800]

Any video of lowering concentration of HF acid to below 5%

[@ambition8800]

@@vibzzlab but it's easily available in hardware shops but if possible I wish to support u thanks

[@illya.ruslanovichshevchenk4106]

Can NaClO be used instead of NaBrO?

[@illya.ruslanovichshevchenk4106]

@@vibzzlab Thank you for the answer.

[@kobold7763]

@@vibzzlab how much naoci should be used? An equimolar amount to bromine, minus the molar mass of sodium?

[@shahyarexperiments9082]

Can we get acetic anhydride from acetamide?

[@noodlesoup2281]

@@vibzzlab really? I’m not entirely sure this is true.. if you think you can get it to work do a video! I could imagine it would be pretty popular

[@noodlesoup2281]

@@vibzzlab Doug’s lab ran a ketene lamp for A anhydride on KZbin. I’m pretty sure that has been up there for 6 years! It is an incredibly dangerous route to AA. ketene is not friendly at all, although a relatively simple route to AA. If his has been up for 6 years I can’t see why your vid wouldn’t be okay 🙂. I have scoured literature and forums for an otc prep for a reasonable yielding anhydride synthesis and the best I came up with was the Sulphur chloride route although there are many others they are relatively low yielding and need other exotic Chems which defeats the purpose. I have a feeling if it were that simple to make people wouldn’t resort to ketene nor have 40 page threads discussing feasible routes… That being said I would love to be proved wrong!

[@noodlesoup2281]

@@vibzzlab m.kzbin.info/www/bejne/nWrWgZ-DoL54f9k Check it out!

[@ambition8800]

Can we contact u