Thursday, September 27, 2012

Methylamine Pseudoscience

Pseudoscience strikes again. About a month ago, over at Slate's Brow Beat culture blog, Mr. Daniel Lametti - he of 'Ph.D.-Waste-Of-Time' fame - wrote a piece analyzing a recurring Breaking Bad plot device: the theft of large quantities of methylamine for the characters' illegal methamphetamine operation. The meat of the post:
"As a post on Reddit asks, since Walt is a brilliant chemist, couldn’t he just synthesize the stuff himself?
Yes, and pretty easily. There are many different ways to make the compound; with little more than an introductory organic chemistry class, you could probably synthesize it in your kitchen sink. (Brow Beat doesn’t recommend trying to make methylamine in your kitchen sink). Chemically speaking, methylamine is just ammonia with one hydrogen atom swapped out for a methyl group—a carbon atom and three hydrogen atoms. Without getting into too much detail, an easy way to achieve this swap is to “bubble” ammonia (a gas) through methanol (a liquid) that’s been laced with a dehydrating agent like Silica gel. You could probably buy these chemicals at Home Depot and CVS. Silica gel packets are often packaged with new shoes and electronics to keep them dry."
Wait, huh? Let's start from No.

As a practicing synthetic organic chemist, I agree with the statement that silica gel dehydrates solvents by water absorption. Sure. But I've heated plenty of alcohols in the presence of silica gel, and 99% of them don't spontaneously lose water! (That would be a rocking olefin synthesis, if it worked...)
Methylamine: Easy as hooking up five pressurized reactors in your kitchen sink.
Credit: Albermarle
Let's put this on firm scientific ground. The reaction in question, a nucleophilic substitution, could theoretically occur by two methods: 1. SN1, where the -OH group of methanol dislodges from the methyl cation (?!?!), followed by subsequent ammonia bonding; or 2. SN2, where the ammonia directly displaces the -OH, one step, no intermediates.

In this scenario, both are unlikely, especially at room temperature and pressure.

Now let's talk practicality: which company will sell you a cylinder of ammonia gas for 'home use?' (Not Home Depot). How will you get your methanol? What's the plan to isolate the (volatile, stinky) methylamine from the mixture of compounds this theoretical reaction produces?

OK, how do companies make methylamine? Albemarle technical documents to the rescue! Seems that mixing methanol and excess ammonia at 300-500 degrees Celsius, under pressure, over a zeolite catalyst will produce an equilibrium mixture of methylamine, dimethylamine, and trimethylamine (favored). After fractional distillation, the trimethylamine can be streamed over an amorphous silica / alumina catalyst to disproportionate it back into methylamine.

Not a kitchen sink in sight.

Curious - Appended at the bottom of the essay is a thanks for Prof. Adam Braunschweig, faculty at NYU. To what extent did Prof. Braunschweig proofread this post? Did he sign off on the "kitchen sink silica gel" concept in the middle? I can't possibly imagine that he thoroughly vetted this essay.

4 comments:

  1. That said, methylamine is in fact not so hard to synthesize. Methylamine.HCl can be synthesized via hexamethylenetetramine and conc. HCl & not extremely excessive heating. Perhaps that's a bit closer to a "kitchen sink" procedure.

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    1. Oh, sure, I'll concede that there are ways to get fairly pure compound, and production of the salt would help with isolation / purification. However, I think the transformation discussed in the Slate piece would have issues with selectivity, ease of handling, and reagent sourcing.

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  2. Um, trimethylamine disproportionates into methylamine? What's the other product? Pentamethylamine??

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  3. TMA + NH3 <=> DMA + MMA
    DMA + NH3 <=> 2 MMA

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