Triethylamine → HCID 18979551, compound

Participants

Reaction Conditions

Reaction Steps

0.9 g of triethylamine and then 0.5 g of methanesulphonyl chloride were added dropwise at -25° C. while stirring to a solution of 0.4 g of 3,4-bis(4-[8-acryloyloxyoctyloxy]phenylcarbonyloxy)benzoic acid in 40 ml of tetrahydrofuran. The reaction mixture was stirred at -25° C. for 1 hour, then treated with 0.06 g of 2-fluoro-4-hydroxybenzonitrile and 0.05 g of 4-(dimethylamino)pyridine in 40 ml of tetrahydrofuran, stirred at room temperature overnight, poured into 100 ml of water and then extracted three times with 50 ml of diethyl ether each time. The organic phases were combined, washed twice with 100 ml of water each time, dried over magnesium sulphate, filtered and the filtrate was concentrated. Chromatographic purification of the residue on silica gel with cyclohexane/ethyl acetate (vol. 8:2) and two-fold recrystallization from ethyl alcohol of the fractions which were pure according to thin-layer chromatography gave 1.2 g of 3,4-bis[4-(4-[8-acryloyloxyoctyloxy]phenylcarbonyloxy)phenylcarbonyloxy]-2-fluorobenzonitrile; m.p. (C-I) 85° C., cl.p. (N-I) 3° C.

Provenance & Evidence