反应 #960243

ord-a29f2813bdc541dfb18fcf810d45f2e7

反应方程式

O.OO
hydrogen peroxide water
CC1(C)OB(c2cnc(F)c(F)c2)OC1(C)C
2,3-difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Oc1cnc(F)c(F)c1
title product
收率 29.6%
Oc1cnc(F)c(F)c1
5,6-difluoropyridin-3-ol
收率 29.6%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取extracted with ethyl acetate
  2. 2
    洗涤Combined organic portions were washed with aqueous 5% sodium thiosulfate solution and saturated saline water
  3. 3
    干燥dried over anhydrous sodium sulfate
  4. 4
    浓缩concentrated
  5. 5
    其他Purification via Biotage Spla HPFC system (C18, mobile phase: 0.01% NH4HCO3, CH3CN/water, 10˜95%)

实验过程

A mixture of hydrogen peroxide water (1.50 mL, 13.2 mmol) and 2,3-difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (2.8 g) in tetrahydrofuran (15 mL) was stirred at room temperature for 2 h, then diluted with water and extracted with ethyl acetate. Combined organic portions were washed with aqueous 5% sodium thiosulfate solution and saturated saline water, dried over anhydrous sodium sulfate and concentrated. Purification via Biotage Spla HPFC system (C18, mobile phase: 0.01% NH4HCO3, CH3CN/water, 10˜95%) afforded the title product as a white solid (450 mg).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08975400B2uspto-grants-2015_03