Methyl phenyldiazoacetate is the organic compound with the formula C6H5C(N2)CO2Me. It is a diazo derivative of methyl phenylacetate. Colloquially referred to as "phenyldiazoacetate", it is generated and used in situ after isolation as a yellow oil. Methyl phenyldiazoacetate and many related derivatives are precursors to donor-acceptor carbenes, which can be used for cyclopropanation or to insert into C-H bonds of organic substrates. These reactions are catalyzed by dirhodium tetraacetate or related chiral complexes. Methyl phenyldiazoacetate is prepared by treating methyl phenylacetate with p-acetamidobenzenesulfonyl azide in the presence of base.
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![Methyl phenyldiazoacetate: Solid state structure of tert-butyl diazo(4-nitrophenyl)acetate t-BuO2CC(N2)C6H4NO2, a representative of donor-acceptor carbene precursor related to the title compound. Key distances: C-N = 1.329 Å, N-N = 1.121 Å.[4]](https://upload.wikimedia.org/wikipedia/commons/thumb/6/6c/DOXGON.png/500px-DOXGON.png?utm_source=en.wikipedia.org&utm_campaign=parser&utm_content=thumbnail)
