Journal of Synthetic Organic Chemistry, Japan
Online ISSN : 1883-6526
Print ISSN : 0037-9980
ISSN-L : 0037-9980
Synthesis of 1-Methyl-4-methoxy-7-isopropylnaphthalene
Kazuo ADACHI
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1971 Volume 29 Issue 5 Pages 515-518

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Abstract
1-Methyl-4-methoxy-7-isopropylnaphthalene, 4-methoxy derivative of eudalene, was synthesized from p-cresol. 2-Bromo-4-methylanisole (2) was converted to 2- isopropyl-4- (2-methoxy-5-methylphenyl) butyric acid (9) through ethyl 2-cyano-2-isopropyl-4- (2-methoxy-5-methylphenyl) butyrate (5). The acid chloride of (9) was cyclized with SnCl4 to 2-isopropyl-5-methoxy-8-methyl-1, 2, 3, 4-tetrahydronaphthalen-1-one (10). As isopropyl group was attached at the α-position of the carbonyl group, 2, 4-dinitrophenylhydrazone derivative of (10) was yielded with difficulty. 1-Methyl-4-methoxy-7-isopropylnaphthalene (12) was obtained by reduction of (10) and then heating the product with sulfur.
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© The Society of Syhthetic Organic Chemistry, Japan
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