Josh512 Posted March 23, 2019 Share Posted March 23, 2019 Hi everyone, I have a homework in organic chemistry and I really don't know how to do it so I would be delighted to have your help Here is the exercise : The synthesis of aspartame is carried out according to the following scheme: In a first step, the action of methanol in the presence of hydrogen chloride (HCl) gives compound A in which a single carboxylic acid function has been esterified. This compound A is then reacted with phosgene (COCl2) to give the cyclic product noted B. Propose a mechanism for this transformation from A to B, knowing that phosgene can be considered in this reaction as a double acid chloride (Cl-C(O)-Cl). Link to comment Share on other sites More sharing options...
hypervalent_iodine Posted March 24, 2019 Share Posted March 24, 2019 What have you done so far / where are you stuck? Link to comment Share on other sites More sharing options...
BabcockHall Posted March 28, 2019 Share Posted March 28, 2019 It is often helpful to think in terms of nucleophiles and leaving groups. Link to comment Share on other sites More sharing options...
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