反应详情

123 mg of lithium chloride was suspended in 10 ml of dry tetrahydrofuran under an argon stream, and 0.69 ml of ethyl 2-diethylphosphono-3-methylbutanoate was added under stirring. The mixture was stirred for 5 minutes at room temperature, and then 2.7 ml of a 20% dry tetrahydrofuran solution of diazabicycloundecene was added thereto. The mixture was stirred at room temperature for 10 minutes. Then, 2.0 ml of a dry tetrahydrofuran solution of 773 mg of (4S,5R)-3-benzyloxycarbonyl-2,2-dimethyl-5-formyl-4-isobutyloxazolidine was added thereto, and the mixture was stirred overnight at room temperature. A precipitated inorganic salt was filtered off, and the solvent of the filtrate was distilled off under reduced pressure. The residue was dissolved in 300 ml of benzene and washed with 200 ml of water. The separated aqueous layer was extracted with 75 ml of benzene. The organic solvent layer thus obtained was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (32 g of Kieselgel 60) by using a mixture of hexane/ethyl acetate (10/1) to obtain 623 mg of ethyl 3-[(4S,5S)-3-benzyloxycarbonyl-2,2-dimethyl-4-isobutyloxazolidin-5-yl]-2-isopropyl-2-propenoate as a colorless oily substance.

1. additionwas added
2. stirringThe mixture was stirred for 5 minutes at room temperature
3. stirringThe mixture was stirred at room temperature for 10 minutes
4. stirringthe mixture was stirred overnight at room temperature
5. filtrationA precipitated inorganic salt was filtered off
6. distillationthe solvent of the filtrate was distilled off under reduced pressure
7. dissolutionThe residue was dissolved in 300 ml of benzene
8. washwashed with 200 ml of water
9. extractionThe separated aqueous layer was extracted with 75 ml of benzene
10. customThe organic solvent layer thus obtained
11. dry with materialwas dried over anhydrous magnesium sulfate
12. distillationThen, the solvent was distilled off under reduced pressure
13. customthe residue was purified by silica gel column chromatography (32 g of Kieselgel 60)
14. additiona mixture of hexane/ethyl acetate (10/1)