反应详情

In a manner analogous to Example 1, 52.5 g of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalene-carboxylic acid were converted by reaction with 200 ml of thionyl chloride into the acid chloride and, after dissolution in 200 ml of tetrahydrofuran, added dropwise to a solution of 48.8 g of 4-[2-(4-amino-phenoxy)ethyl]-morpholine in 400 ml of pyridine while cooling slightly. The temperature should not rise above 30° C. After stirring at room temperature for 1 hour the reaction mixture was poured on to ice-water, extracted with ethyl acetate, the organic phase was washed with ice-cold 2N hydrochloric acid, dried and evaporated. The crystalline crude product was purified by filtration over a silica gel column (eluting agent hexane/ethyl acetate 1:4, then ethyl acetate, then ethyl acetate/ethanol =1:1) and recrystallized from hexane/ ethyl acetate. There were obtained 52 g of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-4'-(2-morpholinoethoxy)-2-naphthalenecarboxanilide in white crystals. m.p. 134° C.-136° C.

1. temperaturewhile cooling slightly
2. customrise above 30° C
3. extractionextracted with ethyl acetate
4. washthe organic phase was washed with ice-cold 2N hydrochloric acid
5. customdried
6. customevaporated
7. filtrationThe crystalline crude product was purified by filtration over a silica gel column (
8. washeluting agent hexane/ethyl acetate 1:4
9. customethyl acetate, then ethyl acetate/ethanol =1:1) and recrystallized from hexane/ ethyl acetate