反应详情

温度

10 °C

n-Butyl lithium (508 microL, 2.5 M/hexanes, 3.0 equivalents) was added dropwise (1 drop every 5 seconds) to an oxygen degassed solution of 4-Bromo-2-(4-ethoxy-benzyl)-1-fluoro-benzene (392.0 mg, 1.27 mmol) in anhydrous tetrahydrofuran (1.5 mL) at −78° C. under nitrogen. The resulting solution was stirred at this temperature for 1 hour. Then a solution of (2R,3S,4S)-2,3,4-tris-benzyloxy-5-hydroxy-6-(4-methoxy-benzyloxy)-5-(4-methoxy-benzyloxymethyl)-hexanoic acid methoxy-methyl-amide I-1g (330.0 mg, 0.423 mmol) in anhydrous tetrahydrofuran (0.75 mL) was added dropwise very slowly (1 drop every 5 seconds) and the resulting mixture was stirred at −78° C. for an additional hour before warming to 10° C. over 12 hours (put in a deep Dewar covered with aluminum foil to maintain cold temperature). The reaction was diluted with diethyl ether and quenched by the dropwise addition of aqueous 1N hydrochloric acid solution. The resulting biphasic mixture was stirred at room temperature for 15 minutes. The organic phase was separated, washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified by flash chromatography over silica gel (eluting with a gradient of 10 to 40% ethyl acetate in heptane) to afford the product as a mixture of isomers (180 mg, 44% yield).

1. stirringthe resulting mixture was stirred at −78° C. for an additional hour
2. temperatureto maintain cold temperature)
3. customquenched by the dropwise addition of aqueous 1N hydrochloric acid solution
4. stirringThe resulting biphasic mixture was stirred at room temperature for 15 minutes
5. customThe organic phase was separated
6. washwashed with brine
7. dry with materialdried over magnesium sulfate
8. filtrationfiltered
9. concentrationconcentrated under reduced pressure
10. customThe crude residue was purified by flash chromatography over silica gel (
11. washeluting with a gradient of 10 to 40% ethyl acetate in heptane)
12. customto afford the product
13. additionas a mixture of isomers (180 mg, 44% yield)