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Synthesis of Substituted Resorcinol Monomethyl Ethers from 2-Bromo-3-methoxycyclohex-2-en-1-ones
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- Author(s) / Creator(s)
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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
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- Subjects / Keywords
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- Type of Item
- Article (Draft / Submitted)