HRID227751

反应详情

EQUATION

反应方程式

HRID 227751 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

In a 250 mL round bottom flask was dissolved 3-(bromomethyl)-2-chloropyridine (7.2 g, 35 mmol) in MeOH (70 mL). To the solution was added sodium cyanide (3.4 g, 70 mmol), then attached a reflux condenser, stirred the mixture at 80° C., while monitoring the reaction by LCMS. After about 1.5 h, the reaction was cooled to RT, concentrated, diluted with EtOAc, upon which a white solid crashed out. The solids were filtered and rinsed with EtOAc. The organic filtrate was concentrated to yield a crude reddish brown solid. The solid was dissolved in EtOAc, and purified by silica gel chromatography eluting with 40-70% EtOAc/Hexanes. The product fractions were concentrated to yield 2-(2-chloropyridin-3-yl)acetonitrile as an off-white solid. MS m/z=153 [M+1]+. Calc'd for C7H5ClN2: 152.58.

WORKUP

后处理

  1. customthe reaction by LCMS
  2. temperaturethe reaction was cooled to RT
  3. concentrationconcentrated
  4. additiondiluted with EtOAc, upon which a white solid
  5. filtrationThe solids were filtered
  6. washrinsed with EtOAc
  7. concentrationThe organic filtrate was concentrated
  8. customto yield a crude reddish brown solid
  9. custompurified by silica gel chromatography
  10. washeluting with 40-70% EtOAc/Hexanes
  11. concentrationThe product fractions were concentrated