Issue 3, 2003

Reaction between naphthols and dimethyl acetylenedicarboxylate in the presence of phosphites. Synthesis of stable oxa-2λ5-phosphaphenanthrenes, and benzochromene derivatives

Abstract

The reaction of dimethyl acetylenedicarboxylate (DMAD) with 2-naphthol in the presence of trimethyl or triphenyl phosphite leads to stable dimethyl oxa-2λ5-phosphaphenanthrene derivatives in good yields. The reaction of DMAD and trimethyl phosphite in the presence of 1-naphthol or 8-hydroxyquinoline leads to dimethyl 2-(dimethoxyphosphoryl)-3-(1-hydroxy-2-naphthyl)succinate or dimethyl 2-(dimethoxyphosphoryl)-3-(8-hydroxyquinolin-7-yl)succinate in excellent yields. Using triethyl phosphite and DMAD in the presence of 2-naphthol or 1-naphthol produces methyl 3-oxo-2,3-dihydro-1H-benzo[f]chromene-1-carboxylate or methyl 2-oxo-3,4-dihydro-2H-benzo[h]chromene-4-carboxylate in excellent yields.

Graphical abstract: Reaction between naphthols and dimethyl acetylenedicarboxylate in the presence of phosphites. Synthesis of stable oxa-2λ5-phosphaphenanthrenes, and benzochromene derivatives

Article information

Article type
Paper
Submitted
18 Oct 2002
Accepted
28 Nov 2002
First published
14 Jan 2003

Org. Biomol. Chem., 2003,1, 560-564

Reaction between naphthols and dimethyl acetylenedicarboxylate in the presence of phosphites. Synthesis of stable oxa-2λ5-phosphaphenanthrenes, and benzochromene derivatives

I. Yavari, M. Anary-Abbasinejad and Z. Hossaini, Org. Biomol. Chem., 2003, 1, 560 DOI: 10.1039/B210263N

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