화학공학소재연구정보센터
Chemistry Letters, Vol.31, No.3, 278-279, 2002
Enhanced leaving ability of methoxy group and retarded deprotonation on the carbon atom linked to the 1-position of 8-phosphino- or 8-amino-naphthalene
In an attempt to lithiate a benzylic carbon, a benzyl methyl ether bearing an 8-phosphino-1-naphthyl group at the benzylic carbon is treated with t-butyllithium to result in the formation of a quite unexpected compound, arising not from deprotonation but from the removal of the methoxy group accompanied by the introduction of two t-butyl groups into the naphthalene ring.