反应 #2348089

ord-4ecf643ab25c4906a12ec5cd57602a18

反应方程式

OO
hydrogen peroxide
Cc1cc(F)c(F)c(OB(O)O)c1
compound ( 3 )
Cc1cc(F)c(F)c(OB(O)O)c1
2,3-difluoro-5-methylphenylboric acid
Cc1cc(O)c(F)c(F)c1
2,3-difluoro-5-methylphenol

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度Under cooling with an ice bath
  2. 2
    workup.DISSOLUTIONhaving been dissolved in 300 mL
  3. 3
    温度Under cooling with an ice bath
  4. 4
    其他to terminate
  5. 5
    其他the reaction
  6. 6
    萃取The aqueous layer was extracted with diethyl ether, which
  7. 7
    workup.ADDITIONwas added to the organic layer
  8. 8
    洗涤the organic layer was washed with a saturated sodium hydrogensulfite aqueous solution
  9. 9
    干燥a saturated saline and then dried over anhydrous magnesium sulfate
  10. 10
    workup.DISTILLATIONThe solvent was distilled off in vacuo

实验过程

Under cooling with an ice bath, 53.1 g of aqueous hydrogen peroxide was slowly added dropwise to the compound (3) having been dissolved in 300 mL, followed by stirring at room temperature for 3 hours. Under cooling with an ice bath, 100 mL of a saturated sodium hydrogensulfite aqueous solution was added dropwise thereto to terminate the reaction. The aqueous layer was extracted with diethyl ether, which was added to the organic layer, and the organic layer was washed with a saturated sodium hydrogensulfite aqueous solution and a saturated saline and then dried over anhydrous magnesium sulfate. The solvent was distilled off in vacuo to obtain 22.7 g of 2,3-difluoro-5-methylphenol (4).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07846513B2uspto-grants-2010_12