反应 #710496

ord-5a9b73d27a68401e8f7b11a019189fc7

反应方程式

OCc1cnc(C(F)(F)F)cc1Cl
[4-Chloro-6-(trifluoromethyl)pyridin-3-yl]methanol
O=S(Cl)Cl
SOCl2
FC(F)(F)c1cc(Cl)c(CCl)cn1
4-chloro-5-(chloromethyl)-2-(trifluoromethyl)pyridine
收率 87.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the mixture was refluxed for 1 hour
  2. 2
    浓缩The mixture was concentrated
  3. 3
    workup.ADDITIONthe residue was poured into water (1 L)
  4. 4
    萃取The mixture was extracted with ethyl acetate (500 mL*3)
  5. 5
    浓缩The combined organic layer was concentrated

实验过程

[4-Chloro-6-(trifluoromethyl)pyridin-3-yl]methanol (Int-12) (90 g, 0.426 mol) was added to SOCl2 (700 mL) slowly with ice bath, the mixture was refluxed for 1 hour. The mixture was concentrated and the residue was poured into water (1 L). The mixture was adjusted to pH=7-8 with solid NaHCO3. The mixture was extracted with ethyl acetate (500 mL*3). The combined organic layer was concentrated to yield 4-chloro-5-(chloromethyl)-2-(trifluoromethyl)pyridine (Int-13) (80 g, 87%) as brown syrup which was used for the next step without further purification.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09301526B2uspto-grants-2016_04