HRID77112

反应详情

EQUATION

反应方程式

HRID 77112 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
35 °C

PROCEDURE

实验过程

A mixture of (3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)methanol (2.1 g, 8.64 mmol), TEMPO (0.094 g, 0.604 mmol), and a sodium phosphate buffer (0.67M) (32.2 mL, 21.59 mmol) in acetonitrile (30 mL) was heated to 35° C. A fresh solution of sodium phosphate buffer (40 mL, pH ˜6.5) consisting of a 1:1 solution of NaH2PO4 (20 mL, 0.67M) and Na2HPO4 (20 mL, 0.67M) was prepared and used. Solutions of sodium chlorite (3.91 g, 34.5 mmol) in water (4.5 mL) and bleach (4.3 mL, 6% wt.) were added simultaneously over 40 min. The reaction was monitored by HPLC, and after 2 h, ˜30% of the starting material remained. After 6 h, 10% remained. Additional bleach (100 μL) was added, and the reaction mixture was left at room temperature overnight. Additional bleach (100 μL) was added. The resulting mixture was allowed to stir at 35° C. for additional 2 h. HPLC indicated complete conversion. The reaction was quenched by the slow addition of a solution of sodium sulfite (2.07 mL, 43.2 mmol) in water (90 mL) at 0° C., resulting in the disappearance of the brown reaction color. The solvent was removed under reduced pressure, and the remaining aqueous residue was extracted with ethyl acetate (3×40 mL). The organic layers were combined, washed with water (8 mL), washed with brine (8 mL), and dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded 3-phenyl-4-(trifluoromethyl)isoxazole-5-carboxylic acid (2.2 g, 8.55 mmol, 99% yield) as a pale yellow solid.

WORKUP

后处理

  1. customwas prepared
  2. additionwere added simultaneously over 40 min
  3. waitAfter 6 h
  4. additionAdditional bleach (100 μL) was added
  5. waitthe reaction mixture was left at room temperature overnight
  6. additionAdditional bleach (100 μL) was added
  7. customresulting in the disappearance of the brown reaction color
  8. customThe solvent was removed under reduced pressure
  9. extractionthe remaining aqueous residue was extracted with ethyl acetate (3×40 mL)
  10. washwashed with water (8 mL)
  11. washwashed with brine (8 mL)
  12. dry with materialdried over anhydrous sodium sulfate
  13. concentrationConcentration under reduced pressure