HRID491421

反应详情

EQUATION

反应方程式

HRID 491421 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Ref.: WO 96/11917. A slurry of 2,6-dinitro phenol (20% in H2O, 5 g, 0.0271 mol), NH4Cl (14.30 g, 0.267 mol), and ammonium hydroxide solution (3 mL) was heated in a 70° C. bath. A warm solution of Na2S-9H2O (24.19 g, 0.1 mol) in H2O (23 mL) was added to the slurry and the resulting orange suspension was heated with stirring for 3 h, then allowed to cool to room temperature. The mixture was cooled in an ice bath and slowly acidified with 6 N HCl to pH 2. The mixture was filtered and the filtrate was extracted with CHCl3 (3×75 mL). The combined organic extracts were concentrated in vacuo and the crude material was adsorbed onto silica gel. Purification by silica gel chromatography, eluting with 25% hexane/CH2Cl2 then CH2Cl2, afforded the title compound (1.47 g) as a brick red powder. MS (ESI-POS): [M+H]+=155.

WORKUP

后处理

  1. temperaturethe resulting orange suspension was heated
  2. temperatureThe mixture was cooled in an ice bath
  3. filtrationThe mixture was filtered
  4. extractionthe filtrate was extracted with CHCl3 (3×75 mL)
  5. concentrationThe combined organic extracts were concentrated in vacuo
  6. customPurification by silica gel chromatography
  7. washeluting with 25% hexane/CH2Cl2