Journal
ADVANCED SYNTHESIS & CATALYSIS
Volume 352, Issue 10, Pages 1667-1676Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201000092
Keywords
C-H activation; iron catalysis; oxidation; phosphonation; regioselectivity
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Funding
- Chinese Scholarship Council
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The dehydrogenative alpha-phosphonation of substituted N,N-dialkylanilines by dialkyl H-phosphonates was achieved under mild conditions by using environmentally benign iron(11) chloride as catalyst and tert-butyl hydroperoxide as oxidant. The reaction proceeded in the presence of electron-donating (methoxy, methyl, benzyl) and electron-withdrawing ring-substitutents (bromo, carbonyl, carboxyl, m-nitro) in moderate to good yields. The X-ray crystal structure of N-(5,5-dimethy1-2-oxo-2 lambda(5)-[1,3,2]dioxaphosphinan-2-yl-methyl)-N-methyl-p-tol-uidine was determined. Bis-(4-(dimethylamino)phenyl)methane and bis-4,4'-(dimethylamino)benzophenone underwent bisphosphonation selectively by respective monophosphonation at the remote dimethylamino groups. Furthermore, the use of excess dialkyl H-phosphonate and oxidant allowed us to functionalize both methyl groups of N(CH3)(2) in N,N-dimethyl-p-toluidine and N,N-dimethylaminomesidine, respectively, to obtain alpha,alpha'-bisphosphonatoamines in high yield.
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