HRID481937

反应详情

EQUATION

反应方程式

HRID 481937 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 5'-O-dimethoxytritylthymidine (27.23 g, 50.0 mmol) in pyridine (100 mL) at 0° C. was added phenoxyacetyl chloride (8.23 mL, 62.5 mL) dropwise, and the mixture was allowed to warm to ambient temperature over 3 hr. The reaction was quenched with methanol (ME, 25 mL) and concentrated in vacuo. The crude product was extracted with dichloromethane (DCM, 300 mL), washed with saturated aqueous sodium bicarbonate (SASB, 300 mL), dried (Na2 SO4), and concentrated. Toluene (2×100 mL) was added, and the solution was concentrated. The residual oil was dissolved in 10% ME in DCM (275 mL) and treated with methanesulfonic acid (3.24 mL, 50.0 mmol). After 30 min the red solution was quenched with SASB (300 mL), and the organic layer was dried (Na2SO4) and concentrated. The crude product was dissolved in 1:1 ethyl acetate (EA): hexanes (H) (250 mL) and precipitated by cooling to -10° C. for 18 h. The mixture was filtered, and the precipitate dried under vacuum to afford 1 (11.4 g, 60.6%). 1H NMR δ 13C NMR (D6DMSO) δ 12.25, 36.41, 61.29, 64.59, 75.57, 83.68, 84.41, 109.75, 114.52, 121.23, 129.48, 135.77, 150.45, 157.54, 163.65, 168.42. HRMS (FAB) calcd. C18 H21N2O7 (MH+) 377.1349; found 377.1355.

WORKUP

后处理

  1. customThe reaction was quenched with methanol (ME, 25 mL)
  2. concentrationconcentrated in vacuo
  3. extractionThe crude product was extracted with dichloromethane (DCM, 300 mL)
  4. washwashed with saturated aqueous sodium bicarbonate (SASB, 300 mL)
  5. customdried (Na2 SO4)
  6. concentrationconcentrated
  7. additionToluene (2×100 mL) was added
  8. concentrationthe solution was concentrated
  9. dissolutionThe residual oil was dissolved in 10% ME in DCM (275 mL)
  10. customAfter 30 min the red solution was quenched with SASB (300 mL)
  11. dry with materialthe organic layer was dried (Na2SO4)
  12. concentrationconcentrated
  13. dissolutionThe crude product was dissolved in 1:1 ethyl acetate (EA)
  14. customhexanes (H) (250 mL) and precipitated
  15. temperatureby cooling to -10° C. for 18 h
  16. filtrationThe mixture was filtered
  17. customthe precipitate dried under vacuum