Syntheses based on cyclohexadienes. Part 2. Convenient synthesis of 6-alkylsalicylates, 6-alkyl 2,4-dihydroxybenzoate, and 2,5-dialkylresorcinols


Autoria(s): Charles, Kanakam C; Neelakandha, Mani S; Halasya, Ramanathan; Subba, Rao GSR
Data(s)

1989

Resumo

A one pot synthesis of 6-alkylsalicylates and 6-alkyl-2,4- dihydroxybenzoates is described. Cycloaddition of 1-methoxycyclohexa-1,4- or 1,3-dienes with alkylpropiolic esters results in the regio-specific formation of 2-alkyl-6-methoxybenzoates. Thus, methyl 2-methoxy-6-methyl benzoate, methyl 2,4-dimethoxy-6-methylbenzoate, methyl 2,5-dimethoxy-6-methylbenzoate, methyl 2-methoxy-4,6-dimethylbenzoate, and ethyl 2-butyl-4,6-dimethoxybenzoate, have been prepared. By making use of this method, the synthesis of two dihydroisocoumarins namely (±)-mellein (12) and (±)-6-methoxy- mellein (14) is described. Employing a similar strategy, a novel route to 2,5-dialkylresorcinols has been developed. Stemphol (24b) and the antibiotic DB2073 (24d) have been synthesized.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/30369/1/syn.pdf

Charles, Kanakam C and Neelakandha, Mani S and Halasya, Ramanathan and Subba, Rao GSR (1989) Syntheses based on cyclohexadienes. Part 2. Convenient synthesis of 6-alkylsalicylates, 6-alkyl 2,4-dihydroxybenzoate, and 2,5-dialkylresorcinols. In: Journal of the Chemical Society, Perkin Transactions 1 (11). pp. 1907-1913.

Publicador

Royal Society of Chemistry

Relação

http://www.rsc.org/publishing/journals/P1/article.asp?doi=p19890001907

http://eprints.iisc.ernet.in/30369/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed