It turns out that there's another synthesis route to acetic anhydride that requires more equipment but uses more accessible chemicals. Acetone. I had an idea for the synthesis of the commonly used, but hard to obtain reagent acetic anhydride. KMnO4 oxidises primary alcohols to their. Read 5 answers by scientists with 4 recommendations from their colleagues to the question asked by Atul R Bendale on Dec 10,


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Acetic anhydride

In order to remove the last portions of the water, the salt is heated further with a large flame, until the solidified mass melts for the second time. To 70 grams of finely pulverized, anhydrous sodium acetate are placed in round bottom flask equipped with dropping funnel and distillation condenser connected with receiving flask protected from moisture with calcium chloride tube.

Due to its low cost, acetic anhydride is usually acetic anhydride synthesis, not prepared, for use in research laboratories.

Reactions[ edit ] Acetic anhydride is a versatile reagent for acetylationsthe introduction of acetyl groups to organic substrates. It was recycled to the reactor.

Crude acetic anhydride suitable for further refining was removed from the lower portion of the acetic anhydride synthesis.

The lower boiling components methyl acetate, methyl acetic anhydride synthesis and some acetic acid were taken overhead and fed to a tank to which makeup methyl acetate was also fed. The contents of the tank were continuously fed to the reactor feed line.

A completely OTC ;) acetic anhydride synthesis , Hive Chemistry Discourse

The data thus accumulated is shown in Table I. The hydrogen in the gas feed was stopped at hour and was resumed at hour As indicated by the conversion and space-time yield data in Table I, there was no significant tar formation during the period of time when hydrogen gas was fed to acetic anhydride synthesis reactor.

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The data of Table I show that discontinuing the hydrogen feed to the carbonylation reactor has a substantial detrimental effect on production rate, i.

The duration of the first run was 64 hours, the second In Runshigh space-time yields were obtained although the higher concentrations of hydrogen resulted in the formation of significant amounts of ethylidenediacetate.

Also, in these runs, the tar formation was minimal and acetic anhydride synthesis be easily handled. acetic anhydride synthesis

Synthesis of acetic anhydride

In Run 4, essentially no ethylidenediacetate was formed but the space-time yield of acetic anhydride was decreased considerably by the use of only 1. You can also tell from the full procedure and from the name "anhydride", resembling "anhydrous", meaning acetic anhydride synthesis water Thus, any conditions that would allow for esterification of acetic acid would also cause esterification of salicylic.

And so now you have the situation that we talked about up here. Your carboxylate anion functions as a nucleophile, attacks your electrophilic carbon on your acyl chloride.

So we could show these electrons attacking this carbon, these electrons kick off onto the oxygen, and then when those electrons move back in, to reform your double bond, these electrons would kick off onto your chlorine, and acetic anhydride synthesis so we can go acetic anhydride synthesis and draw our product.

So just thinking about what happens in this mechanism, we can go ahead and draw our products, which would be a symmetical anhydride, so we would have our oxygen right here, and then we would have our group over here.

So thinking about the R groups this time, so this R group is a methyl group, and then we could think about this oxygen being this oxygen, and then this portion of the acyl chloride is this portion for our final product for our acid anhydride.


And so this is acetic anhydride, which is the one that's used most commonly in an undergraduate lab. And so this is a nice way of preparing acid anhydrides. Let's look at another way to form acetic anhydride. You could start with two carboxylic acids, and this would be acetic acid and acetic acid, so the same carboxylic acid, and apply high acetic anhydride synthesis, and this time you think about a dehydration reaction, so you could think about losing an OH from one, and a hydrogen from the other, to form water, so you acetic anhydride synthesis think about losing a water here, and your dehydration reaction.