HRID38990

反应详情

EQUATION

反应方程式

HRID 38990 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Two batches of [(2R)-7-bromo-2,3-dihydro-1,4-benzodioxin-2-yl]methanol (2.2 g, 8.9 mmol), sodium methanesulfinate (85%) (1.6 g, 13.3 mmol), CuI (0.2 g, 0.9 mmol), L-proline (0.2 g, 1.8 mmol) and K2CO3 (0.2 g, 1.8 mmol) in DMSO (20 ml) were heated under microwave radiation at 140° C. for 3 h in nitrogen-flushed vials. Water and EtOAc were added. The water layer was extracted with EtOAc (3×100 ml) and the combined organic phases were washed with LiCl (5%), HCl (1 N) and brine. The resulting solution was dried (Na2SO4) and evaporated to dryness. The residue was purified by flash column chromatography (isooctane/EtOAc) to give the title compound (1.7 g). MS m/z (rel. intensity, 70 eV) 244 (M+, bp), 213 (39), 165 (26), 134 (22), 79 (23).

WORKUP

后处理

  1. customflushed vials
  2. additionWater and EtOAc were added
  3. extractionThe water layer was extracted with EtOAc (3×100 ml)
  4. washthe combined organic phases were washed with LiCl (5%), HCl (1 N) and brine
  5. dry with materialThe resulting solution was dried (Na2SO4)
  6. customevaporated to dryness
  7. customThe residue was purified by flash column chromatography (isooctane/EtOAc)