反应 #682203

ord-d33b94c7759147c1ac79f786402c6809

反应方程式

Nc1c(F)cc(C=O)c(F)c1Br
4-amino-3-bromo-2,5-difluorobenzaldehyde
O=N[O-].[Na+]
sodium nitrite
CCOC(C)=O
ethyl acetate
O=Cc1cc(F)cc(Br)c1F
3-bromo-2,5-difluorobenzaldehyde
收率 44.1%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cooling
  2. 2
    萃取the aqueous phase extracted with DCM
  3. 3
    干燥The combined organic phases were dried over sodium sulfate
  4. 4
    其他evaporated

实验过程

4-amino-3-bromo-2,5-difluorobenzaldehyde (3.4 g, 14.3 mmol) was dissolved in acetic acid (18 mL) before addition of hypophosphoric acid (50% in water, 39 mL). A solution of sodium nitrite (1.4 eq, 1.4 g) in water (8 mL) was then added dropwise under ice-cooling. After stirring at rt for 2 h, the reaction mixture was poured onto a mixture ice/water and the aqueous phase extracted with DCM. The combined organic phases were dried over sodium sulfate and evaporated. A column chromatography (0 to 10% ethyl acetate in petroleum ether) afforded 3-bromo-2,5-difluorobenzaldehyde (1.3 g, 6.3 mmol, 44%). 1H NMR (d6-DMSO) δ 10.15-10.12 (m, 1H), 8.13 (ddd, J=8.0, 5.0, 3.0 Hz, 1H), 7.66 (ddd, J=8.0, 5.0, 3.0 Hz, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09242987B2uspto-grants-2016_01