acetoacetate synthesis. More than one step may be required. Provide all reagents needed (2) Propose how to obtain the following compound using either malonic ester synthesis or for each step and product after each step

Ochem question: Provide the stepwise mechanism for the synthesis of the following compound via an enamine  (see attached image)

Please give the appropriate reagents to complete the following synthesis. 1 2 3

Provide a synthesis for the following reaction. If more than one step is required be sure to number separate steps.

Benzocaine (ethyl p amino benzoate) is a local anesthetic compound. Design its synthesis from toluene using the necessary reagents.

The Stork reaction is a condensation reaction between an enamine donor and an a,ẞ-unsaturated carbonyl acceptor. The overall reaction consists of a three-step sequence of 1. formation of an enamine from a ketone. 2. Michael addition to an α,ß-unsaturated carbonyl compound, and 3. hydrolysis of the enamine in dilute acid to regenerate the ketone. Consider the Stork reaction between cyclohexanone and propenal. Draw the structure of the product of the enamine formed between cyclohexanone and dimethylamine. ચર્ચ F Correct HC, CH3 ChemDoodle 2 Draw the structure of the Michael addition product. ChemDoodle Jn (F 106 Correct

Suggest a synthesis of the following compound by using the acetoacetic ester synthesis. Show all required reagents.

How to synthesize phenyl methyl bromide?

2) Propose a synthesis of the following using 3-buten-2-one acetoacetic ester synthesis.