Difunctional derivatives of bis(<i>m</i>-phenylene)-32-crown-10

Abstract

Optimization studies of the condensation of methyl 3,5-dihydroxybenzoate (1) with tetra(ethylene glycol) dichloride (3) resulted in improvement of the yield of the 1 + 1 cyclization product, 5-carbomethoxy-m-phenylene-16-crown-5 (5), to 67% (HPLC), but no improvement in the yield (28%, HPLC) of the desired 2 + 2 product, bis(5-carbomethoxy-m-phenylene)-32-crown-10 (4). However, after optimization, a two-step procedure provided improved yields of 4 and this procedure was generalized to afford other difunctional monomers. Condensation of substituted resorcinols with 3 and subsequent transformations yielded substituted (R) 3,5-bis(11-chloro-3,6,9-trioxaundecyl-oxy)benzenes (7, 9–14). Reaction of dihalides 7 (R = COOCH 3 ), 13 (R = CHO), and 12 (R = CH 2 OSi(Me) 2 -t-Bu) with methyl 3,5-dihydroxybenzoate (1) produced bis(5-carbomethoxy-m-phenylene)-32-crown-10 (4) (43%), 5-carbomethoxy-m-phenylene-5′-formyl-m′-phenylene-32-crown-10 (15) (32%), and the lactone (16a) (18%, derived from the initially formed 5-hydroxymethyl-m-phenylene-5′-carbomethoxy-m′-phenylene-32-crown-10 (16)), respectively. Subsequent reactions gave the corresponding diacid (17), bis(hydroxymethyl) (19), bis(bromomethyl) (20), diacetyl (18), diformyl (21), bis(p-nitrophenoxymethyl) (22), and di(acetoxymethyl) (23) derivatives. Keywords: cyclization, functionalized bis(m-phenylene) crown ethers.