HRID1244048

反应详情

EQUATION

反应方程式

HRID 1244048 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-70 °C

PROCEDURE

实验过程

A solution of 0.63 g (3.5 mmol) 3-methoxy-6-nitro-2-vinyl-pyridine in 50 ml of CH2Cl2 and 10 ml of methanol was cooled to −70° C. Ozone was bubbled into the solution until a blue color persisted. The mixture was stirred for 60 minutes at −70° C. and then quenched with excess dimethyl sulfide. The reaction was warmed to room temperature and the solvent evaporated. The residue was dissolved in ethyl acetate and water. The pH of the solution was adjusted to 2.0 with 1N HCl and the mixture stirred for 30 minutes. The pH of the solution was then adjusted to 8.0 with 1N NaOH. The mixture was extracted with excess ethyl acetate. The ethyl acetate extracts were combined, dried (Na2SO4) and evaporated to yield 0.6 g of 3-methoxy-6-nitro-pyridine-2-carbaldehyde as a tan solid. TLC. Rf=0.2 (1.1 ethyl acetate/hexane). 1H NMR (CDCl3) δ 10.1 (s, 1H), 8.5 (d, 1H), 7.85 (d, 1H), 4.15 (s, 3H).

WORKUP

后处理

  1. customOzone was bubbled into the solution until a blue color
  2. customquenched with excess dimethyl sulfide
  3. temperatureThe reaction was warmed to room temperature
  4. customthe solvent evaporated
  5. dissolutionThe residue was dissolved in ethyl acetate
  6. stirringthe mixture stirred for 30 minutes
  7. extractionThe mixture was extracted with excess ethyl acetate
  8. dry with materialdried (Na2SO4)
  9. customevaporated