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Corrosive Chemistry
Canada
Приєднався 15 лис 2016
Exploring chemistry and showing some unique reactions
Preparation of 6-Bromo-2-naphthol from 2-Naphthol
The bromination of 2-naphthol to form the intermediate 1,6-dibromo-2-naphthol, followed by the reduction with metallic tin to 6-bromo-2-naphthol.
Procedure: Koelsch, C.; Bachmann, W.; Kushner, S. 6-Bromo-2-naphthol. Org. Synth. 1940, 20, 18. DOI: 10.15227/orgsyn.020.0018
www.orgsyn.org/demo.aspx?prep=CV3P0132
Vanillin stain formulation: www.chemistry.mcmaster.ca/adronov/resources/Stains_for_Developing_TLC_Plates.pdf
Patreon: www.patreon.com/corrosion
Procedure: Koelsch, C.; Bachmann, W.; Kushner, S. 6-Bromo-2-naphthol. Org. Synth. 1940, 20, 18. DOI: 10.15227/orgsyn.020.0018
www.orgsyn.org/demo.aspx?prep=CV3P0132
Vanillin stain formulation: www.chemistry.mcmaster.ca/adronov/resources/Stains_for_Developing_TLC_Plates.pdf
Patreon: www.patreon.com/corrosion
Переглядів: 2 139
Відео
Cholesteryl Acetate Preparation, Analysis, and Polarimetry
Переглядів 2,2 тис.Рік тому
The preparation of cholesteryl acetate from cholesterol. Procedure from: www.orgsyn.org/demo.aspx?prep=CV2P0191 (Note 7) Patreon: www.patreon.com/corrosion
Fenbufen Synthesis
Переглядів 3,9 тис.Рік тому
In this video, I demonstrate the synthesis of the NSAID fenbufen, a compound taken off the market a few years ago due to concerns over liver toxicity. Procedure taken from Sittg's pharmaceutical manufacturing encyclopedia. www.patreon.com/corrosion
Succinic Anhydride Synthesis
Переглядів 4,5 тис.Рік тому
Fenbufen Part 2/3. Here's a quick preparation video. The dehydration of succinic acid to succinic anhydride using acetic anhydride following the procedure described in Vogel's Practical Organic Chemistry. Patreon: www.patreon.com/corrosion Music: Waltz of the Flowers - Tchaikovsky, Audio Library
Biphenyl Preparation from Bromobenzene
Переглядів 6 тис.Рік тому
Fenbufen Part 1/3. The coupling of phenylmagnesium bromide using copper(II) chloride to form biphenyl. Be careful when drying the copper(II) chloride so you don't get oxychloride formation and a 31% yield! Patreon: www.patreon.com/corrosion Music: C Major Prelude, Bach
Synthesis of a Selenium Heterocycle 2,1,3-Benzoselenadiazole
Переглядів 2,9 тис.Рік тому
Preparation of 2,1,3-benzoselenadiazole from o-phenylenediamine and selenous acid. I made this just because I thought it was a cool looking heterocycle. There aren't too many practical applications for this compound. Procedure references: pubmed.ncbi.nlm.nih.gov/885962/ pubs.rsc.org/en/content/articlelanding/1990/an/an9901501441/ Patreon: www.patreon.com/corrosion
2-Methoxynaphthalene from 2-Naphthol
Переглядів 8 тис.2 роки тому
The methylation of 2-naphthol to prepare 2-methoxynaphthalene. Two different procedures are demonstrated in this video, one from Vogel with dimethyl sulfate and the other with methyl iodide (iodomethane) using a general (and somewhat lazy) Williamson ether synthesis. 2-Methoxynaphthalene is used as a pleasant-smelling perfume ingredient and a chemical building block. Preparation of 2-naphthol f...
2-Naphthol Synthesis from Naphthalene
Переглядів 9 тис.2 роки тому
First sodium naphthalene-2-sulfonate is prepared by the sulfonation of naphthalene at 165 °C. The sodium naphthalene-2-sulfonate is then fused with molten potassium hydroxide at 300-310 °C, then the 2-naphtholate is acidified forming 2-naphthol. Music: Hungarian Rhapsody No 2 - Liszt ua-cam.com/video/ZuzLFxfv_Zc/v-deo.html www.patreon.com/corrosion
Morpholine Preparation from Diethanolamine
Переглядів 8 тис.2 роки тому
The synthesis of morpholine from diethanolamine. Morpholine Procedure: 62.5 g of diethanolamine is added to a round bottom flask with a thermocouple and air condenser. Concentrated hydrochloric acid is added until a pH of 1 is reached (~50-60 mL of HCl). The diethanolamine hydrochloride solution is heated, driving off the water until an internal temperature of 200-210 °C is reached, this temper...
Triphenylbismuth Synthesis
Переглядів 17 тис.3 роки тому
The preparation of triphenylbismuth by the transmetallation between bismuth trichloride and phenylmagnesium bromide. www.patreon.com/corrosion
Synthesis of p-Methylacetophenone
Переглядів 27 тис.3 роки тому
In this video, I follow another procedure from Vogel on the Friedel-Crafts acylation of toluene with acetic anhydride to produce p-methylacetophenone. Music: Serenade for Strings, Elgar
Synthesis of Dicinnamalacetone
Переглядів 7 тис.4 роки тому
The synthesis of dicinnamalacetone via a double aldol condensation of cinnamaldehyde with acetone. I plan to use this compound in an upcoming video if the next couple of steps in the total synthesis work out well.www.patreon.com/corrosion Music: "Olivier" by Wintergatan Build Tracks This track can be downloaded for free at www.wintergatan.net Free License to use this track in your video can be ...
Knorr Pyrrole Synthesis of Knorr's Pyrrole
Переглядів 8 тис.4 роки тому
In this video I show the Knorr pyrrole synthesis of 3,5-diethoxycarbonyl-2,4-dimethylpyrrole, also known as diethyl 3,5-dimethylpyrrole-2,4-dicarboxylate, also known as simply Knorr's pyrrole. This is a nice one pot reaction with 32.5g of ethyl acetoacetate, 75mL of glacial acetic acid, 8.7g of NaNO2, and 16.7g of zinc. www.patreon.com/corrosion
Synthesis of 3,5-Dimethylpyrazole
Переглядів 13 тис.4 роки тому
In this video I follow the procedure in Vogel's practical organic chemistry on the synthesis of 3,5-dimethylpyrazole by the condensation of hydrazine with acetylacetone. Correction: When I listed the melting point range for the product from the chloroform extraction I said 105 to 1-O-10 C when I meant 105-110 C www.patreon.com/corrosion
Proline Decarboxylation to Pyrrolidine
Переглядів 6 тис.4 роки тому
The acetophenone catalyzed decarboxylation of proline to pyrrolidine. Pyrrolidine is a useful reagent in organic synthesis due to its reaction with carbonyl groups to form enamines. The Sciencemadness thread: www.sciencemadness.org/whisper/viewthread.php?tid=64791#pid633399 A paper on the reaction: pubs.rsc.org/en/content/articlelanding/1968/j3/j39680000406 Patreon: www.patreon.com/corrosion
Sucrose Octaacetate Synthesis, An Intensely Bitter Compound
Переглядів 3,4 тис.4 роки тому
Sucrose Octaacetate Synthesis, An Intensely Bitter Compound
The Synthesis of 1,2,3,4-Tetrahydrocarbazole
Переглядів 15 тис.4 роки тому
The Synthesis of 1,2,3,4-Tetrahydrocarbazole
Simple Aniline Synthesis from Vitamin B10
Переглядів 8 тис.5 років тому
Simple Aniline Synthesis from Vitamin B10
Synthesis of 1,4-Dibromobutane from THF
Переглядів 8 тис.5 років тому
Synthesis of 1,4-Dibromobutane from THF
Making an Organometallic Ruthenium Complex (p-Cymene Ruthenium Dichloride Dimer)
Переглядів 6 тис.5 років тому
Making an Organometallic Ruthenium Complex (p-Cymene Ruthenium Dichloride Dimer)
Synthesis of Cobalt Triphenylphosphine Complexes
Переглядів 8 тис.5 років тому
Synthesis of Cobalt Triphenylphosphine Complexes
Tetrakis(pyridine)silver Dichromate Preparation
Переглядів 2 тис.5 років тому
Tetrakis(pyridine)silver Dichromate Preparation
I'm doing this prep (the methyl iodide one but with sodium hydroxide if I can get it to disolve 🙏), thanks for this video. You should see the Indian school teacher video of this handling dimethyl sulfate, no gloves, no funeral hood like it's nothing. Sorry auto wrong, I meant to say fume hood 😆
These videos are great!!
The KOH reflux and filtration pulls out traces of distilled water, are MgSO4, CaCl2 or NaOH suitable for aniline?
😊
Thank you For you effort and time ! I've been told Ferrocene synthesis is a test of skill (even though we routinely use ultra low liquid Nitrogen temperatures in labs which are way tougher). I sure learned a lot by your video. Its so heartening to know so many Chemists like this author upload detailed videos such as this; though they may never be monetised. I salute you friend. I am located in Pune India . You truly are one of the many Gems which occasionally get discovered.
Interesting experience. 1-naphthoic acid, are you not interested in this synthesis? it would be a great experiment.
I want to talk to you
oh man , you work with some toxic things ! and i thought the guy that built a ketene lamp was crazy ...
If I didn't crystallize at least 3 times, I couldn't stop :) If you want purity, you have to make an effort. This is a great post, I follow your work with pleasure. Are you an academic?
I just recently did this synthesis, it was really cool! Now I need to deal with the waste, any tips?
sir can I have the mechanism for this reaction please
Dissolve a bit of lithium metal in 100ml of methanol. You'll end up with a methanolic solution of lithium methoxide which burns with a beautiful crimson red flame. The contrast between burning trimethyl borate and lithium methoxide is simply gorgeous.
What is this used for?
Very nice. Did you add a stabilizer or were you using it quickly? Something like hydroquinone or tert-butylcatechol? Also did you ever check the concentration? I think this method is a good solution for me I am just curious how it worked out for you in the end?
Thankyou for posting this video btw.
I didn’t add any stabilizer, just stored the aniline in an amber bottle away from light, over time the aniline will darken regardless. I didn’t do a titration to determine the exact concentration/purity but it should be quite pure after distillation. Many other people have replicated my procedure (there are some other videos posted about this reaction on UA-cam now) and they have had good results as well!
What do you mean due to the loss of vacuum in the system? Dont you keep the vacuum pump running during the distillation? Or do you pull the vacuum, close the system then run the heat to distill product? I always thought they say to keep the vacuum pump running during the whole process and have a vacuum constantly pulling on the atmosphere inside the system? Im confused lol
Is it a must to use concentrated sulfuric acid??? Can i replace it with diluted one 37%???
Do you by any chance know if you can make acetic anhydride by reacting succinic anhydride with acetic acid? It's something i have been asking myself for quite some time now, i just don't have the time to experiment myself lately.
This channel is very underrated
I'm confused why you called the step of mixing with HCl "quenching". I see how that's where you're moving from one phase to another in the procedure, but the real quench IMO was when you turned the hot plate off, since this was a pyrolysis. The other way this could be quenched was if you were deactivating the reagents with HCl, but the catalyst would be unaffected.
wouldnd also just bromobenzene with sodium work in a wurtz reaction?
5:19 that type of adapter is actually called just "cow", because it looks like an udder.
Wow bro uploaded nearly a year later 😂😂, Great workup and thanks.
Need
Very pretty!
This compound is very useful.
Liszt! Brilliant music! And chemistry!!!! 👍
Any synthesis that contains toluene is amazing! 👍And beautiful music!
Any synthesis that includes acetic anhydride I click away from. Why watch something that is basically banned.
Awesome
Congratulations to you for reaching 5k! Well done, I was happy with your results and the analysis was well documented too. I do wonder if there would be interest in some glassware cleaning ASMR? ^^
Amazing upload as usual!
Graham would be Proud!
Always a pleasure when you upload. Few, but ripe; one does not weigh gemstones on a grocery scale. Your videos are worthy of emulation.
With the large difference in Rf between the desired product and the unknown non-polar impurity, it might make sense to run a column long enough to discard that first fraction. It's a lot of material to process though at this scale.
Quite professionally made synthesis. I'm happy to see such good quality and understanding of the process. 👏👍
Very nice and original synthesis, love to see new stuff on yt
This was a great synthesis!
Awesome, well done!
Nice work
6:44 H3O?
would this reaction also work with phenylethynyl magnesium bromide?
Hello, could you give a video tutorial on the synthesis of triethylene glycol ditmethacrylate (CAS 109-16-0) and DIURETHANE DIMETHACRYLATE, MIXTURE OF ISOMERS (CAS 72869-86-4)
hello, if i have hydrazine hydrate, how much to use and do i need water ond NaOH ?
the smell of naphthalene is too repugnant for recreational chemistry. Leave naphthalene to the industrialists.
Hello!In the last step at 9:36 there is a dehydrogenation reaction with Pb3O4. Do you have a citation for this reaction?
I didn't supose that methyl sulphate is so toxic.
I love your video, what is the name of that book you have?
Interesting and thanks. A lot of dyes are made with aniline.
Это же наркотики!!!!! Ужас!!!!
MD
One use I found was as a starting material for the total synthesis of chlorophyll A, which I'm sure involves a tremendous amount of work as the intermediate chlorin-e6 trimethyl ester took 46 separate steps to produce according to the summary of the paper.
😊