تفاعل #1366
ord-dd7b84cd2bdd41c8acecfbb08583d7c0
معادلة التفاعل
sodium hydroxide
2,4,5-trifluoroaniline
dimethyl sulfide
N-chlorosuccinimide
→
2-methylthiomethyl-3,4,6-trifluoroaniline
الكواشف
لا شيء
المذيبات
ظروف التفاعل
درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىis gradually added below 5° C
- 2درجة الحرارةAfter reflux for 12 hours
- 3استخلاصextracted with dichloromethane
- 4تجفيفthe extract is dried over sodium sulfate
- 5تركيزconcentrated
- 6أخرىThe residue is purified with column chlomatography (silica-gel, dichloromethane: n-hexane=1:4)
الإجراء التجريبي
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).