Chemistry of Heterocyclic Compounds

, Volume 9, Issue 4, pp 501–502 | Cite as

Reaction of diazomethane with some α-substituted acrylates

  • V. R. Likhterov
Article
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Abstract

The reaction of methyl α-methoxy-, α-acetoxy-, and α-chloroacrylate with diazomethane proceeds in conformity with the -M orienting effect of the ester group. The resulting Δ1-pyrazolines are converted to 3(5)-carbomethoxypyrazole at room temperature (the reaction proceeds more readily on heating).

Keywords

Methyl Ester Organic Chemistry Acrylate Ester Group 

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Copyright information

© Consultants Bureau 1975

Authors and Affiliations

  • V. R. Likhterov

There are no affiliations available

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