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Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: dolphinsea14 on April 24, 2018, 12:41:13 PM

Title: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on April 24, 2018, 12:41:13 PM
Hi everyone,
I am synthesizing ferrocene, for that purpose I need cyclopentadiene. I have a question and would be very thankful if you could help me.
Can cracking and distillation of dicyclopentadiene to cyclopentadiene be done without nitrogen atmosphere?
Thanks in advance :)
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: pgk on April 24, 2018, 01:13:41 PM
Yes, you can but it is not recommended for safety reasons.
1). Both dicyclopentadiene and cyclopentadiene are highly flammable.
2). Besides, the high distillation temperature favors their oxidation in air and will decrease the distillation yield.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on April 24, 2018, 01:41:36 PM
Yeah, I know that it can be dangerous, but I had no idea how much. We don't have nitrogen at university, that's why I asked if it could be done without it.
Thank you very much :)
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on April 24, 2018, 01:46:44 PM
Can you suggest good way to synthesize nitrogen for inert atmosphere, and dry it?
I was thinking about using gas bubbler containing concentrated sulfuric acid, will it be enough to get clean and dry nitrogen? Or can it be done using silica gel?  Is there another way it could be done? (I have no much experience I'm doing a synthesis on my own for the first time, I had to design it myself, please help...)
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: pgk on April 24, 2018, 01:54:12 PM
No, don’t do that. You are going to combine a dangerous technique with another and more dangerous one.
Alternatively, you can distill small amounts of dicyclopentadiene, in the lab fume with a closed safety screen and under adequate ventilation.
But take care and pay attention for any ignition source, nearby.

Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on April 24, 2018, 02:04:15 PM
So there is no way I can synthetize nitrogen and conduct it in the destillation apparatus? This is how it should look like...
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: Arkcon on April 24, 2018, 02:11:48 PM
Try to get a small tank of clean, dry nitrogen.  It is literally cheaper than air.  That's not a joke, they will actually sell you a tank of nitrogen for less than a tank of air; economy of scale, demand and supply, etc.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on April 24, 2018, 02:31:45 PM
Yeah, that would be great, but I can't buy it, I am a student at college, in country like ours finding and buying chemicals as student, is not that simple. It's a bit complicated...
However, I need a way to synthesize nitrogen and conduct it. Buying is not an option.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: Borek on April 24, 2018, 03:30:05 PM
If you are doing it as a part of your course it is not up to you to buy the chemicals, it is up to the school to provide you with the necessary reagents and hardware. Have you talked with your supervisor?
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: Arkcon on April 24, 2018, 03:48:59 PM
You could also get another school to lend you a nitrogen generator, basically a system that pulls air over an oxygen consuming reagent and gives you clean dry nitrogen.

When a chemist needs nitrogen, they get it from a tank or the atmosphere.  Finding the most energetic nitrogenous compound, and decomposing it, carefully, to get nitrogen gas is beating a wasp's nest with a stick because you need a sheet of paper.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on April 24, 2018, 04:05:32 PM
Yes, of course I talked to my supervisor and to the lab assistant. I asked for nitrogen. They said I will have to synthesize it, because we don't have nitrogen.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on April 24, 2018, 04:11:18 PM
I know Arkcon, that's true, I totally agree, but unfortunately things in Macedonia don't work that way. It's a bit  silly, they ask us to make something, don't have all the necessary stuff, so we have to make our own solutions, find alternatives. Sad, but true.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: clarkstill on April 25, 2018, 03:57:03 AM
Finding the most energetic nitrogenous compound, and decomposing it, carefully, to get nitrogen gas is beating a wasp's nest with a stick because you need a sheet of paper.

that is an outstanding metaphor
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: Enthalpy on April 25, 2018, 04:59:24 AM
Could clean argon be easier to find in your university? It serves for welding.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: wildfyr on April 25, 2018, 01:52:06 PM
Purposefully generating nitrogen from a solid is reasonably similar to setting off an explosive on purpose. Have you heard of ammonium nitrate or azide explosions? Those are examples of generating nitrogen from a solid.

We aren't trying to pile on, we are just telling you, with the weight of decades of experience among the respondents, that it is very very dangerous to try to make nitrogen in situ like that, and finding nitrogen already in gas form is so much easier and better in every single way. Argon would work too.

Do you have a biology department? They often use liquid nitrogen. If you can get that you can get some you can add it in small amounts to an attached container and it should supply N2 to a reaction. It sure is more cumbersome than just a tank. OR you may be able to charge a gas tank off the liquid nitrogen container.

Heres an odd angle that I can't find a counterargument to aside from price. What about helium? They have it in party stores. You could buy a whole bunch of balloons...please shoot me down if I'm missing something obvious.

Another note about the sulfuric acid bubbler: that removes water, not O2 which is what you are trying to exclude.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on April 25, 2018, 03:20:42 PM
Thank you very much, everyone, for all the good advice, I really appreciate your help.
I guess I will try some of these solutions, and I hope everything will turn out well. :)
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: Enthalpy on April 26, 2018, 04:45:32 AM
If supplying from party balloons, just make sure their helium isn't mixed with hydrogen. It's often done to save cost. As long as the mix isn't flammable in air, it saves precious helium.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on April 26, 2018, 12:44:32 PM
Ok, thank you Enthalpy :)
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: billnotgatez on April 26, 2018, 11:10:35 PM
As for Helium

My understanding ( and it may be wrong)
The party balloon cylinders are mixed with air as a safety precaution because people have been known to inhale from those cylinders to get Donald Duck voice .
Although some new reserves have been found, industrial Helium source have become more pricey since the deregulation of prices and the loosening of the requirement to extract from natural gas.

I have often thought that there was a slight bit of some kind of oil or impurities in various gas cylinders that were used for industrial purposes and not medical.

I was going to price check the difference between Argon and Nitrogen but lost patience.

In any case [not to hijack this thread]
Why use nitrogen rather than Argon?
Is it just price?
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: OrganicDan96 on April 27, 2018, 02:52:14 PM
what about CO2 you can make that really easily in the lab. or might it be too reactive?
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: rolnor on April 28, 2018, 02:02:21 PM
You can remove oxygen from air by bubbling it through a alkaline solution of pyrogallol.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: Borek on April 28, 2018, 02:30:48 PM
You can remove oxygen from air by bubbling it through a alkaline solution of pyrogallol.

Traces of oxygen, yes, but if one needs a lot of gas the idea is way too costly. Bubblers make sense when you want to clean technical argon or nitrogen from oxygen impurities, not when you deal with the normal air.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: rolnor on April 28, 2018, 06:10:53 PM
You can remove oxygen from air by bubbling it through a alkaline solution of pyrogallol.

Traces of oxygen, yes, but if one needs a lot of gas the idea is way too costly. Bubblers make sense when you want to clean technical argon or nitrogen from oxygen impurities, not when you deal with the normal air.

But how much does he need, is it not sufficient to fill the apparatus?
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: zarhym on May 02, 2018, 05:21:23 AM
I have done this reaction before at about several hundred grams scale. I didn't use nitrogen since the reaction/distillation was done at reduced pressure. The cracking temperature of was around 180°C to 220°C. The strategy of this reaction is very simple.  Once the dimer was cracked into monomer, the desired product goes into gas phase at this temperature under reduced pressure, then being collected in the condenser. The reaction and separation happens simultaneously.

Since the apparatus of this approach is always under reduced pressure, there is very limited amount of oxygen is the gas phase. This oxygen can react with diene. But it only generate very small amount of impurities, which was not a problem to me.

You can add small amount of polymerization inhibitor such as tert-butyl catechol. It was good for this reaction.

The diene (with trace amount of TBC stabilizer) was stable in freezer for several days (tested with HNMR) in my case.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: pgk on May 02, 2018, 11:21:40 AM
This is a convenient and rather safe technique. The addition of an antioxidant such as BHT, BHA, TBC (this one), etc. is a smart idea, too.
But even so, vacuum must be slowly broken, otherwise atmospheric oxygen will violently penetrate into the glassware.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on May 02, 2018, 01:58:14 PM
I did it that way too, zarhym, without nitrogen, and it went well.
I didn't need much, I collected few mililiters. I was performing microsynthesis of ferrocene so I needed 0,3mL.
I got some orange particles floating in the beaker, but after vacuum filtration, the precipitate was completely brown (I guess impurities are present) What do you think?  The filtrate was dark blue, that means it contains ferrocenium ion, doesnt't it? How can I recover ferrocene from filtrate? Should I use SnCl2(as a reducing agent) or do you have other suggestions?
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: dolphinsea14 on May 02, 2018, 02:01:27 PM
And is it necessary to remove filter paper before sublimation (using petri dish and beaker with ice on the top)? The temperature should be less than 100 degrees Celsius.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: zarhym on May 08, 2018, 12:11:43 AM
The attachment is the HNMR spectrum of cyclopentadiene I obtained.
Without inert gas protection, my next step synthesis using cyclopentadiene at this purity is still messy.

There are simply too many side reactions of cyclopentadiene under air, which are competitive to your ferrocene synthesis. Beside, iron(II) ion can be oxidized into iron(III), which may be a problem to your reaction. Although synthesis cyclopentadiene may not need nitrogen protection, I highly recommend that you use cyclopentadiene under nitrogen atmosphere.

I also have no idea if ferrocene is stable in air. It looks like the orange particles you have is not very stable. The color change may indicate oxidization since there is large amount air being pulled through the filtration cake.

To avoid this oxidization, I may try the filtration in a glovebox (nitrogen atmosphere). This will eliminate the influence from oxygen and water.
Also, I may try recrystallize the ferrocene. If the ferrocene is in its crystalline form rather than amorphous solid, it should be more robust in the air.

Good luck.
Title: Re: Cracking of Dicyclopentadiene to Cyclopentadiene
Post by: wildfyr on May 08, 2018, 09:26:20 AM
Ferrocene is pretty stable in air whenever I've used it. Also, https://www.sciencedirect.com/topics/chemistry/ferrocene.