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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
Received
11 January 2005
Publication Date:
02 May 2005 (online)
Publication History
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
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Zaitsev AB.Vasil’tsov AM.Schmidt EYu.Mikhaleva AI.Morozova LV.Afonin AV.Ushakov IA.Trofimov BA. Tetrahedron 2002, 58: 10043 - 2
Weissermel K.Arfe HJ. Industrial Organic Chemistry 3rd ed.: VCH; Weinheim: 1997. p.358 - 3
Wilson K.Adams DJ.Rothenberg G.Clark JH. J. Mol. Catal. A: Chem. 2000, 159: 309 - 4
Quin LD. A Guide to Organophosphorus Chemistry Wiley-Interscience; New York: 2000. - 5
Trost BM.Dake GR. J. Am. Chem. Soc. 1997, 119: 7595 - 6
Trost BM.Kazmaier U. J. Am. Chem. Soc. 1992, 114: 7933 - 7
Trost BM.Li C. J. Am. Chem. Soc. 1994, 116: 3167 - 8
Rafel S.Leahy JW. J. Org. Chem. 1997, 62: 1521 - 9
Yavari I.Ramazani A. Synth. Commun. 1997, 27: 1449 - 10
Yavari I.Norouzi-Arasi H. Phosphorus, Sulfur Silicon Relat. Elem. 2002, 177: 87 - 11
Nair V.Rajesh C.Vinod AU.Bindu S.Sreekanth AR.Mathess JS.Balagopal L. Acc. Chem. Res. 2003, 36: 899