HRID1186210

反应详情

EQUATION

反应方程式

HRID 1186210 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

A mixture of 2-bromo-5-difluoromethyl-pyridine (1.8 g, 8.9 mmol) [Lemoine, R. C. et al., Bioorg. Med. Chem. Lett. (2010), 20(16), 4753-56], palladium(II)acetate (19.9 g, 0.089 mmol), triethylamine (9.4 ml, 66.7 mmol) and 1,3-bis(diphenyphosphino)propane (361 mg, 0.89 mmol) in a 2:1-mixture of dry methanol and dimethylsulfoxide (32.5 ml) was heated at 60° C. in an autoclave at 600 psi of carbonmonoxide pressure. After heating for 24 hours, the reaction mixture was cooled and the solid was filtered off. The filtrate was concentrated at reduced pressure to afford the crude product. Ethyl acetate (60 ml) was added and the solution washed successively with water (3×15 ml) to remove the dimethylsulfoxide. After drying over sodium sulphate and concentration at reduced pressure the crude material (5.0 g) was purified by column chromatography using a 1:4-mixture of ethyl acetate and hexane as the eluent. The 5-difluoromethyl-pyridine-2-carboxylic acid methyl ester was obtained as a light yellow oil (1 g, 63% of theory).

WORKUP

后处理

  1. temperatureAfter heating for 24 hours
  2. temperaturethe reaction mixture was cooled
  3. filtrationthe solid was filtered off
  4. concentrationThe filtrate was concentrated at reduced pressure
  5. customto afford the crude product
  6. washthe solution washed successively with water (3×15 ml)
  7. customto remove the dimethylsulfoxide
  8. dry with materialAfter drying over sodium sulphate and concentration at reduced pressure the crude material (5.0 g)
  9. customwas purified by column chromatography