反应 #1366

ord-dd7b84cd2bdd41c8acecfbb08583d7c0

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他is gradually added below 5° C
  2. 2
    温度After reflux for 12 hours
  3. 3
    萃取extracted with dichloromethane
  4. 4
    干燥the extract is dried over sodium sulfate
  5. 5
    浓缩concentrated
  6. 6
    其他The residue is purified with column chlomatography (silica-gel, dichloromethane: n-hexane=1:4)

实验过程

To 2,4,5-trifluoroaniline (35.0 g) are added anhydrous dichloromethane (530 ml) and dimethyl sulfide (24.6 ml) and the mixture is cooled to 0° C. Thereto N-chlorosuccinimide (38.2 g) is gradually added below 5° C. After the mixture is stirred at the same temperature for 15 minutes, triethylamine (47.7 ml) is gradually added. After reflux for 12 hours, the resultant is made alkaline with 5% aqueous sodium hydroxide solution, extracted with dichloromethane, and the extract is dried over sodium sulfate and concentrated. The residue is purified with column chlomatography (silica-gel, dichloromethane: n-hexane=1:4) to give 2-methylthiomethyl-3,4,6-trifluoroaniline (22.3 g).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723648uspto-grants-1998_03