反应详情

Under argon flow, 1.45 g of 5-(3-bromobenzyl)-2,2-dimethyl-1,3-dioxane was dissolved in 7 ml of dry tetrahydrofuran, and cooled with the dry ice-acetone bath. To the mixture was added 0.9 ml of N,N,N′,N′-tetramethylethylenediamine, and then n-butyllithium (1.6 M hexane solution) was added dropwise at −60° C. or less. After 10-minute-stirring, a suspension of 1.03 g of tri-n-butylphosphine and 0.97 g of copper iodide/7 ml of dry tetrahydrofuran was added and the mixture was stirred for 10 minutes. A solution of 1.52 g of 4-iodomethyl-5-methyl-2-phenyloxazole/7 ml of dry tetrahydrofuran was added dropwise at −60° C. or less, and the mixture was stirred for 15 minutes under the same conditions. The bath was removed and the mixture was stirred for 1.5 hours. To the reaction solution was added saturated aqueous ammonium chloride solution. The mixture was diluted with water, extracted with ether, filtrated to remove insolubles, washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (Wakogel® C-200, n-hexane: ethyl acetate=4:1) to provide 0.34 g of the objective compound as white crystals. M.p. 85-87° C.

1. additionwas added
2. stirringthe mixture was stirred for 10 minutes
3. stirringthe mixture was stirred for 15 minutes under the same conditions
4. customThe bath was removed
5. stirringthe mixture was stirred for 1.5 hours
6. additionTo the reaction solution was added saturated aqueous ammonium chloride solution
7. additionThe mixture was diluted with water
8. extractionextracted with ether
9. filtrationfiltrated
10. customto remove insolubles
11. washwashed with water
12. dry with materialdried over anhydrous magnesium sulfate
13. concentrationconcentrated
14. customThe residue was purified by silica gel column chromatography (Wakogel® C-200, n-hexane: ethyl acetate=4:1)