反应 #2200604

ord-6f919ce58c7341598185eaf429a5b63f

反应方程式

OC(CCl)c1ccccc1
2-chloro-1-phenylethanol
Cc1ncsc1C
4,5-dimethylthiazole
Cc1sc[n+](CC(O)c2ccccc2)c1C.[Cl-]
product
Cc1sc[n+](CC(O)c2ccccc2)c1C.[Cl-]
3-(2-Phenyl-2-hydroxyethyl)-4,5-dimethylthiazolium chloride

溶剂

反应条件

温度
135°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度were heated
  2. 2
    温度It was cooled to room temperature
  3. 3
    workup.STIRRINGwith stirring
  4. 4
    萃取was extracted with ether (30 mL)
  5. 5
    workup.ADDITIONThe water layer was treated with actived carbon
  6. 6
    其他evaporated to dryness
  7. 7
    其他It was crystallized from a mixture of acetonitrile and ether

实验过程

The neat mixture of 2-chloro-1-phenylethanol (2.34 g, 14.9 mmol) and 4,5-dimethylthiazole (1.69 g, 14.9 mmol) were heated with stirring at 135° C. for 28 hrs. It was cooled to room temperature and water (30 mL) was added to the reaction mixture with stirring, and then was extracted with ether (30 mL). The water layer was treated with actived carbon and evaporated to dryness. It was crystallized from a mixture of acetonitrile and ether to give a racemic product as prisms; 0.39 g (9.7%); mp. 201-203° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07432254B2uspto-grants-2008_10