Organic chemistry

Imp April 11, 2025 6:17 am

The ML needs to go through Friedan Crafts Alkylation and then be converted into a carboxcyljc acid using Benzyllic oxidation and then an acid chloride using SOCl2.

He’s done NOTHING except being a partial Reduction of ester to an aldehyde using DIBAL and water. Maybe he could’ve been created using Vilsmeyer Haack Reaction but either way he ends up on ketone in para position to the EDG!

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