反応 #53961
ord-8082524e776e4a49acc1e360c46e8567
反応方程式
反応物
試薬
反応条件
後処理
- 1workup.STIRRINGthe resulting mixture was stirred at −78° C. for an additional 1 h
- 2温度the mixture was warmed to room temperature
- 3その他The organic layer was separated
- 4抽出the aqueous layer was extracted with ethyl acetate (3 times)
- 5洗浄washed with saturated sodium chloride aqueous solution
- 6乾燥dried over magnesium sulfate
- 7ろ過filtered
- 8濃縮concentrated
- 9その他The residue was chromatographed (flash column, silica gel, methylene chloride:methanol:diethyl ether=90:2:8)
実験手順
A solution of tert-butyl ((4R)-2-benzhydryl-4-phenyl-oxazolidin-3-yl)-acetate (3.0 g, 6.98 mmole, obtained from Reference Example 10) in anhydrous terahydrofuran (86 ml) was cooled at −78° C. under argon. A solution of lithium diisopropylamide (2M solution in heptane/tetrahydrofuran/ethylbenzene, Aldrich) was added dropwise over a period of 10 min, and the resulting orange solution was stirred at −78° C. for 1 h. A solution of isobutyraldehyde in anhydrous tetrahydrofuran (10 ml) was added to the cooled reaction mixture via syringe, and the resulting mixture was stirred at −78° C. for an additional 1 h. Saturated sodium bicarbonate aqueous solution was added, and the mixture was warmed to room temperature. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate (3 times). The extracts were combined, washed with saturated sodium chloride aqueous solution, dried over magnesium sulfate, filtered and concentrated. The residue was chromatographed (flash column, silica gel, methylene chloride:methanol:diethyl ether=90:2:8) to give (2S,3S)-2-((4R)-2-benzhydryl-4-phenyl-oxazolidin-3-yl)-3-hydroxy-4-methyl-pentanoic acid tert-butyl ester (1.5 g, %) as a pale yellow solid.