# Unusual hydrolysis of methyl 2,4,6‐trimethylbenzoate

Problem 223 from Conceptual Problems in Organic Chemsitry by Singh [1, p. 367]:

The given answer is b and I don't get why. Usual ester hydrolysis would've given a.

I somehow managed to know that the mechanism is SN2, but why? Also, if someone could provide the reaction mechanism, it would be wonderful.

### Reference

1. Singh, D. K. Conceptual Problems in Organic Chemistry: For Engineering and Medical Entrance Examinations, 3rd ed.; Pearson India, 2013. ISBN 978-93-325-8207-1.
• This is a known reaction mechanism for methyl esters with very good leaving groups (more commonly sulfonates, but benzoates as well). Here it's also favored by the steric hindrance of the carbonyl carbon. I'll try to dig up some refs when I have a few more minutes. Jul 19 '20 at 13:31
• Here is a link to a paper that describes the reaction and various examples: folk.ntnu.no/audunfor/7.%20semester/… Jul 19 '20 at 14:47
• @Andrew you should make this an answer as you are undoubtly correct Jul 19 '20 at 20:36
• The problem with this question is that you cannot be sure of the answer a priori. It would be a much better question to present the actual product and ask one to rationalize why that's the case.
– Zhe
Jul 20 '20 at 2:20

In the typical reaction of hydroxide ion with a methyl ester, the hydroxide attacks the carbonyl carbon of the ester, resulting ultimately in elimination of methoxide. Given the basic conditions, the carboxylic acid formed immediately deprotonates to a carboxylate, and the methoxide is protonated to methanol. In older texts particularly, this reaction mechanism is referred to as BAc2, indicating "bimolecular base-catalyzed acyl-oxygen cleavage" (*) because the bond that is broken is between the acyl group and the oxygen of the methoxyl group [see for example Ingold, C.K. (1953) Structure and Mechanism in Organic Chemistry, Cornell Univ. Press].

An alternative mechanism is the BAl2 mechanism, designating "bimolecular base-catalyzed alkyl-oxygen cleavage". As the name suggests, in this mechanism, the bond between the alkyl group and the oxygen is broken. To do this, the hydroxide attacks the methyl carbon in an SN2 reaction, directly yielding the carboxylate and methanol products. This mechanism is also described in detail in Ingold's book and many other sources.

In the years since this mechanism was proposed, there has been some debate about how often it really occurs. Certainly for most esters, BAc2 is the dominant mechanism, and even when reaction by that mechanism is very slow, only a fraction of molecules, if any, react by the BAl2 option.

There seem to be two requirements for the BAl2 type reaction. First, the alkyl group must be methyl or a very ring-strained lactone. Other alkyl groups react much more slowly, as is observed in any SN2 reaction. Second, the carbonyl carbon must be sterically hindered to the point that the BAc2 mechanism is essentially impossible.

I am not certain that the tri-methyl benzoic acid in your question is hindered enough to react exclusively by the BAl2 mechanism, but it is certainly hindered enough that BAc2 would be substantially diminished.

You can find a more thorough discussion of these mechanisms in many textbooks, including the Ingold reference above. Another paper that may be useful is Mueller, P. and Siegfried, B. (1974) SN2 Reactions with Carboxylic Esters. Selective Cleavage of Methyl Esters. Helv Chim Acta 57:987.

*Note that since the net reaction in my example is $$\ce{R-CO2Me + HO- -> R-CO2- + MeOH}$$, the base is a stoichiometric reactant rather than a catalyst, so "base-catalyzed" is a misnomer. That terminology is used because the mechanism is the same if a different nucelophile is used, and the product is a non-acidic acyl derivative rather than a carboxylic acid. In that case, the base is indeed a catalyst.