Long chain phenols. Part 15. Synthesis of 6-n-alkylsalicylic acids (and isomeric acids) from fluoroanisoles with alkyl-lithium
- 1 January 1979
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 8,p. 2079-2087
- https://doi.org/10.1039/p19790002079
Abstract
Various n-alkyl-lithiums have been prepared in ether. They react with both 2- and 3-fluoroanisoles to give, after carbonation, mainly 6-alkyl-2-methoxybenzoic acids. 4-Fluoroanisole gives 2-alkyl-4-methoxybenzoic acids. These reactions probably involve methoxybenzynes and the factors affecting orientation of addition of LiR to these are discussed. Interaction of alkyl-lithium addition products, from 2- and 3-fluoroanisole, with water gave the 3-alkylanisole and, in the case of 4-fluoroanisole, this was accompanied by a small proportion of the 4-alkylanisole. Demethylation of the 6-alkyl-2-methoxybenzoic acids provided syntheses of several naturally occurring anacardic acids.This publication has 3 references indexed in Scilit:
- Long-chain phenols. Part 14. Synthesis of 6-n-alkylsalicylic acids and 3-n-alkylphenolsJournal of the Chemical Society, Perkin Transactions 1, 1979
- Synthesis of 6-[8'-(Z)-pentadecenyl]salicylic acid, "anacardic acid monoene" (ginkgolic acid)The Journal of Organic Chemistry, 1976
- Analgetics Based on the Pyrrolidine Ring. IVJournal of Medicinal Chemistry, 1965