反应 #2200607

ord-f934d52eba7a45a0a1443ed52f903fd9

反应方程式

Cc1ncsc1CO
4-methyl-5-(hydroxymethyl)thiazole
O=C(CCl)c1ccccc1
2-chloroacetophenone
CC#N
Acetonitrile
Cc1c(CO)sc[n+]1CC(=O)c1ccccc1.[Cl-]
3-(2-Phenyl-2-oxoethyl)-4-methyl-5-(hydroxymethyl)thiazolium chloride

反应条件

温度
110°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度the mixture refluxed for another 3 hrs
  2. 2
    温度It was cooled to room temperature
  3. 3
    workup.WAITthe reaction mixture was left overnight at room temperature
  4. 4
    其他The product crystallized
  5. 5
    过滤was filtered
  6. 6
    洗涤washed well with a mixture of hexanes: EtOAc (1:1
  7. 7
    其他v/v) and dried
  8. 8
    其他It was recrystallized from a mixture of acetonitrile/ethanol/ tert-butyl methyl ether

实验过程

The neat reaction of 4-methyl-5-(hydroxymethyl)thiazole (590 mg, 4.57 mmol) and 2-chloroacetophenone (710 mg, 4.59 mmol) was heated at 110° C. The mixture solidified within 15 minutes. Acetonitrile (10 mL) was added and the mixture refluxed for another 3 hrs. It was cooled to room temperature and tert-butyl methyl ether (5 mL) was added and the reaction mixture was left overnight at room temperature. The product crystallized was filtered and washed well with a mixture of hexanes: EtOAc (1:1, v/v) and dried. It was recrystallized from a mixture of acetonitrile/ethanol/ tert-butyl methyl ether; yield 130 mg (10%); mp.240-242° C. (dec.).

来源

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