HRID2215076

反应详情

EQUATION

反应方程式

HRID 2215076 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of alcohol 1-5 (273 mg) in dichloromethane (5 mL) was added Dess-Martin periodinane (451 mg) and the mixture was stirred at room temperature for 1 h and concentrated. The mixture was resuspended in ether, filtered and the filtrate was washed with saturated NaHCO3 and dried over Na2SO4. Filtration and concentration in vacuo afforded the crude aldehyde Ethyl 7-(4-formyl-2-oxo-1,3-oxazolidin-3-yl)heptanoate (1-7) which was used directly without further purification. To a suspension of NaH (47 mg) in THF (6 mL) was added dimethyl 2-oxo-3-phenylpropylphosphonate (282 mg) at 0° C. (formed a white slurry) and the mixture was stirred for an additional 1 h. To the mixture was then added aldehyde 1-7 (145 mg) in THF (4 mL) via cannula and the resultant mixture stirred at room temperature for 2 h and quenched with saturated NH4Cl. The mixture was then extracted with ethyl acetate (3×) and the organic layer was washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by chromatography using ethyl acetate/hexanes (1:1) as the eluent to give the desired product 1-6. 1H NMR (400 mg, acetone-d6): δ 7.36–7.26 (m, 5H), 6.86 (dd, 1H), 6.43 (d, 1H), 4.57 (m, 1H), 4.50 (t, 1H), 4.12–3.96 (m, 5H), 3.28 (m, 1H), 2.96 (m, 1H), 2.28 (t, 2H), 1.65–1.45 (m, 4H), 1.35–1.25, m, 4H), 1.22 (t, 3H).

WORKUP

后处理

  1. concentrationconcentrated
  2. filtrationfiltered
  3. washthe filtrate was washed with saturated NaHCO3
  4. dry with materialdried over Na2SO4
  5. filtrationFiltration and concentration in vacuo
  6. customafforded the crude aldehyde Ethyl 7-(4-formyl-2-oxo-1,3-oxazolidin-3-yl)heptanoate (1-7) which
  7. customwas used directly without further purification
  8. additionTo a suspension of NaH (47 mg) in THF (6 mL)
  9. additionwas added dimethyl 2-oxo-3-phenylpropylphosphonate (282 mg) at 0° C. (
  10. customformed a white slurry) and the mixture
  11. stirringwas stirred for an additional 1 h
  12. customquenched with saturated NH4Cl
  13. extractionThe mixture was then extracted with ethyl acetate (3×)
  14. washthe organic layer was washed with brine
  15. dry with materialdried over Na2SO4
  16. filtrationfiltered
  17. concentrationconcentrated
  18. customThe residue was purified by chromatography