NaK
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Is it possible to perform O-methylations in acetonitrile
I'm having a hard time to find resources on O-alkylations in acetonitrile. I want to use methyl iodide as methylating agent but I don't have good
access to DMF and acetonitrile seems like a suitable replacement. I have considered polarity boiling point and solubility.
Is there something that I missed that would be a problem or prevent this type of reaction work in acetonitrile?
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clearly_not_atara
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It should be fine, I think it's just unpopular because the bp of acetonitrile is kind of low.
In theory a very strong alkylating agent like methyl iodide might form some amount of nitrilium, but even MeI isn't usually strong enough for this so
it shouldn't be a concern. Nitriliums tend to require alkyl triflates or oxoniums.
[Edited on 04-20-1969 by clearly_not_atara]
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karlos³
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Mood: oxazolidinic 8)
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Maybe try NMP, N-methylpyrrolidine?
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NaK
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that's banned because it "may damage the unborn child". Might need to order from outside germany again *sigh*
[Edited on 12-7-2020 by NaK]
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NaK
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Quote: Originally posted by clearly_not_atara  | It should be fine, I think it's just unpopular because the bp of acetonitrile is kind of low.
In theory a very strong alkylating agent like methyl iodide might form some amount of nitrilium, but even MeI isn't usually strong enough for this so
it shouldn't be a concern. Nitriliums tend to require alkyl triflates or oxoniums. |
Shouldn't 82C be more than enough considering the boiling point of MeI is only at 42C?
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Dr.Bob
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ACN works well for alkylating phenols and sulfonamides with MeI and K2CO3, as does acetone and DMF, usually. Sometimes, you can just dump the
reaction into water to ppt the product, much like DMF. Or just filter/decant away from the salts and then evaporate. As noted MeI boils low, so you
almost always need an excess of it to get a complete reaction. If you have a hindered phenol, amide, or other weakly acidic H, you may need to go to
NaH in THF or such. in that case acetone and ACN are not as good.
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clearly_not_atara
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Not exactly -- the volatility of a mixture depends on a number of factors and some high-boiling polar solvents allow methylation at higher
temperatures than would otherwise be possible (NB: I am not the best person to ask about this). It probably isn't a concern for your conditions; I was
just explaining why it isn't typical to use MeCN for this reaction. However, in most cases, it works fine.
[Edited on 04-20-1969 by clearly_not_atara]
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