反応 #951508
ord-c7c8453ffd6a405a93d4bd410e46506d
反応方程式
sodium hydroxide
2,4,5-trifluoroaniline
dimethyl sulfide
N-chlorosuccinimide
→
2-methylthiomethyl-3,4,6-trifluoroaniline
反応条件
温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他is gradually added below 5° C
- 2温度After reflux for 12 hours
- 3抽出extracted with dichloromethane
- 4乾燥the extract is dried over sodium sulfate
- 5濃縮concentrated
- 6その他The residue is purified with column chlomatography (silica-gel, dichloromethane: n-hexane=1: 4)
実験手順
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).