ChemistryGhost
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Will the ester survive?
If someone tried to make an ester out of this and condense the chloride portion of 4-chloro-3-hydroxy-butanal, will the ketone and hydroxide portion
survive? If it does, will the resulting ester survive reductive animation?
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bbartlog
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What reaction are you proposing? Something is supposed to react with the chlorine in your substrate to form an ester? What reaction is that?
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ChemistryGhost
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Reacting the chloride portion with the OH part of something like 1-Naphthol.
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Nicodem
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Quote: Originally posted by ChemistryGhost | If someone tried to make an ester out of this and condense the chloride portion of 4-chloro-3-hydroxy-butanal, will the ketone and hydroxide portion
survive? If it does, will the resulting ester survive reductive animation?
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What ketone? Do you mean an aldehyde?
What ester? Do you mean an ether?
What reductive "animation"? I assume you mean reductive amination instead, but which method?
If you don't know enough of chemical nomenclature to describe the reaction with words, why don't you simply depict it? It is even simpler than using
words and causes less confusion. Also, be specific. I mean, you ask if something will survive some reaction conditions, yet you don't say what
conditions. There are no general reagents and reaction conditions for the reductive amination of aldehydes (there are dozens of reagents and
innumerable reaction conditions). You should also give a review of the published methods used in this and related syntheses. This would greatly
improve the quality of replies.
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