反应详情

A mixture of 58.5 parts of ethyl 7-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylate, 64.25 parts of 2-(3-bromopropoxy) propylbenzene, 17.25 parts of anhydrous potassium carbonate and 1000 parts of acetone was refluxed, with stirring, for 21/2 days and the hot solution filtered. The residue was washed with hot acetone and the combined filtrates evaporated to give an oil which was dissolved in chloroform. The resulting solution was washed with 1N sodium hydroxide solution and then dried. Evaporation of the chloroform gave an oil which yielded a solid on crystallisation from ethanol. The solid was chromatographed on silica gel, eluting with a 1:1 mixture of ethyl acetate and 40/60 light petroleum ether. Evaporation of the eluent and crystallisation of the resulting residue from ethanol gave 18.4 parts of ethyl 4-oxo-7-(3-[2-propylphenoxy]-propoxy)-4H-1-benzopyran-2-carboxylate, m.pt. 75°-76.5°.

1. temperaturewas refluxed
2. filtrationthe hot solution filtered
3. washThe residue was washed with hot acetone
4. customthe combined filtrates evaporated
5. customto give an oil which
6. washThe resulting solution was washed with 1N sodium hydroxide solution
7. customdried
8. customEvaporation of the chloroform
9. customgave an oil which
10. customyielded a solid
11. customon crystallisation from ethanol
12. customThe solid was chromatographed on silica gel
13. washeluting with a 1:1 mixture of ethyl acetate and 40/60 light petroleum ether
14. customEvaporation of the eluent and crystallisation of the resulting residue from ethanol