反応 #53961

ord-8082524e776e4a49acc1e360c46e8567

反応条件

温度
-78°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe resulting mixture was stirred at −78° C. for an additional 1 h
  2. 2
    温度the mixture was warmed to room temperature
  3. 3
    その他The organic layer was separated
  4. 4
    抽出the aqueous layer was extracted with ethyl acetate (3 times)
  5. 5
    洗浄washed with saturated sodium chloride aqueous solution
  6. 6
    乾燥dried over magnesium sulfate
  7. 7
    ろ過filtered
  8. 8
    濃縮concentrated
  9. 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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06858591B2uspto-grants-2005_02