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Synthesis of Substituted Resorcinol Monomethyl Ethers from 2-Bromo-3-methoxycyclohex-2-en-1-ones

  • Author(s) / Creator(s)
  • 2-Bromo-3-methoxycyclohex-2-en-1-ones are readily alkylated at C-6 with
    reactive halides, and then treatment with DBU (2 equiv) in PhMe at room temperature results in
    smooth loss of bromide and aromatization to resorcinol (monomethyl ethers of defined
    substitution pattern.

  • Date created
    2015-01-01
  • Subjects / Keywords
  • Type of Item
    Article (Draft / Submitted)
  • DOI
    https://doi.org/10.7939/r3-75q0-sk96
  • License
    This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Organic Chemistry, copyright © 2015 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.joc.5b02187.
  • Language
  • Citation for previous publication
    • Shao, W., & Clive, D. L. J. (2016). Synthesis of substituted resorcinol monomethyl ethers from 2-bromo-3-methoxycyclohex-2-en-1-ones. Journal of Organic Chemistry, 80(6), 3211–3216. https://doi-org.login.ezproxy.library.ualberta.ca/10.1021/acs.joc.5b00192