Curtius Rearragement

[@MaryHeartMadronal]

THANK YOU 😭💖💖

[@winterwitch6528]

Thanks you so much for the explanation

[@Clutchprep]

You are welcome!!

[@Mohammed-cc5ox]

Thanks For The explanation i think it's better than trying to understand from the book , for the example i think we will do an oxydation to transfer CH3 to CO2H after We ll added Some PCl5 To get COCl and after we gonna use the curtus rearrangement to transform the molecule to anniline

[@Clutchprep]

Hey Zniber! I'm glad you liked the explanation. What you just mentioned is one of the more commonly tested synthetic pathways to make aniline in Organic Chemistry. Its common to oxidize toluene to benzoic acid, then change it to an acid chloride using PCl5 and then (I think you forgot this step) substitute the acid chloride with NaN3 making the acyl azide. Once you have your N3 in place, its easy to do the Curtius and get your aniline.

[@Mohammed-cc5ox]

Yes I forgot to mention that step , Anyway I Hope To Keep Going In This Path You're Doing Great

[@Clutchprep]

Thanks! Feel free to reach out if you have any questions :)

[@rohanrohan4338]

thanks for explanation sir...sir can you plz tell me. how can I convert R-C(O)-NH-NH2 to RNH2 using curtious rxn?..plz sir

[@paranthamanv5609]

You are great

[@Clutchprep]

Thanks for your feedback! Appreciate it! :)