A convenient synthesis of methyl 1-alkoxy-3-perfluoroalkyl-2-naphthoates

DOI: 10.1055/s-1992-26182

Source and publish data:

Synthesis p. 635 - 637 (1992)

Update date:2022-08-05

Topics:

Authors:

Ding Ding

Zhang Zhang

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Article abstract of DOI:10.1055/s-1992-26182

Methyl 1-alkoxy-3-perfluoroalkyl-2-naphthoates 5 were synthesized by heating appropriately substituted 2-triphenylphosphoranylidene-2-butenoates 3 in xylenes at 250°C in a sealed tube. Compounds 3 were obtained via an intramolecular Wittig reaction of 2-alkoxycarbonylbenzyltriphenylphosphonium bromide (1) with methyl 2-perfluoroalkynoates 2 in the presence of potassium carbonate.

Full text of DOI:10.1055/s-1992-26182

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Product name:Benzoic acid, 2-[4-methoxy-4-oxo-2-(trifluoromethyl)-3-(triphenylphosphoranylidene)-1 -butenyl]-, ethyl ester, (E)-

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