HRID1717712

反应详情

EQUATION

反应方程式

HRID 1717712 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Stir a solution of 3-[hydroxy-(4-triisopropylsilanyloxymethyl-phenyl)-methyl]-benzonitrile (12 g, 30.3 mmol), 3,4-dihydro-2H-pyran (3.6 mL, 39.4 mmol) and dichloromethane (250 mL) at room temperature. Add pyridinium p-toluenesulfonate (0.8 g, 3.03 mmol) and stir the resulting mixture 18 hours at room temperature. Dilute the reaction mixture with aqueous saturated sodium hydrogen carbonate (100 mL) and separate the layers. Extract the aqueous layer is washed with dichloromethane (2×50 mL), combine the organic layers, dry with magnesium sulfate, filter and concentrate. Purify the residue via silica chromatography eluting with hexanes to 8:2 hexanes:ethyl acetate to afford the title compound (14.6 g, 100%) as a colorless oil. LCMS (m/z) 478 M−1.

WORKUP

后处理

  1. customseparate the layers
  2. extractionExtract the aqueous layer
  3. washis washed with dichloromethane (2×50 mL)
  4. dry with materialdry with magnesium sulfate
  5. filtrationfilter
  6. concentrationconcentrate
  7. customPurify the residue via silica chromatography
  8. washeluting with hexanes to 8:2 hexanes