SYNTHESIS OF SOME SUBSTITUTED NAPHTHALENES VIA BENZYNE AND THEIR 13C-NMR AND 'H-NMR STUDIES

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چکیده

Aprotic diazotization of anthranilic acid with isoamylnitrite or amylnitrite gave benzenediazonium-2- carboxylate. Subsequent thermal decomposition of this diazonium salt (in situ) in 1,2-dichloroethane as a solvent at 85OC and in the presence of 2,5-diethyl-3,4-diphenylcyclopentadienonaes a trapping agent gave 1,4-diethyl-2, 3-diphenylnaphthalene in high yield, after loss of carbon monoxide. Also, thermal decomposition of this diazonium salt (in situ) was carried out in 1,1 ,2-trichloroethane as a solvent at 108OC in the presence of 2,5-dimethyl-3,4-diphenylcyclopentadienone (monomer) and after loss of carbon monoxide, 1,4-dimethyl- 2,3-diphenylnaphthalene was obtained in excellent yield. These naphthalene derivatives were studied by IR, 'H-NMR, 13C-NMR mass spectra and elemental analysis

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synthesis of some substituted naphthalenes via benzyne and their 13c-nmr and 'h-nmr studies

aprotic diazotization of anthranilic acid with isoamylnitrite or amylnitrite gave benzenediazonium-2- carboxylate. subsequent thermal decomposition of this diazonium salt (in situ) in 1,2-dichloroethane as a solvent at 85oc and in the presence of 2,5-diethyl-3,4-diphenylcyclopentadienonaes a trapping agent gave 1,4-diethyl-2, 3-diphenylnaphthalene in high yield, after loss of carbon monoxide. a...

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عنوان ژورنال:

دوره 4  شماره 2

صفحات  -

تاریخ انتشار 1993-06-01

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