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Synthesis 2005(11): 1761-1764
DOI: 10.1055/s-2005-865359
DOI: 10.1055/s-2005-865359
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Alkyl 3-Aryloxypropenoates and Alkyl 2-Arylacrylates through Nucleophilic Addition to Alkyl Propiolates
Further Information
Publication History
Received
11 January 2005
Publication Date:
02 May 2005 (online)


Abstract
Addition of 1-naphthol, 2-naphthol or 3-hydroxybenzaldehyde to tert-butyl propiolate in the presence of triphenylphosphine leads to tert-butyl 2-arylacrylates and tert-butyl 3-aryloxypropenoates in nearly 1:1 ratio. When phenol, 3-hydroxy-4-methoxybenzaldehyde, 8-hydroxyquinoline or 7-hydroxycoumarin was employed as OH-acid, only alkyl 3-aryloxypropenoates were obtained.
Key words
alkyl propiolates - triphenylphosphine - OH-acid - O-vinylation - C-vinylation