反応 #346135
ord-026a36c5a88347948937c14bcbe3247e
反応方程式
反応物
試薬
反応条件
後処理
- 1workup.STIRRINGthe mixture stirred at room temperature for 3 hours
- 2ろ過At the end of this time period, the reaction mixture was filtered
- 3その他to remove the solids which
- 4その他had precipitated
- 5温度after cooling
- 6その他the solvent was reduced in volume by evaporation under reduced pressure
- 7その他The solids were thereafter removed by filtration
- 8ろ過Additional filtrations
- 9その他gave additional solids
- 10ろ過filtered
- 11その他The solvent was removed by evaporation under reduced pressure
- 12その他dried
- 13その他The 3,4,5-trichloro-N,N-dimethyl-2-((thiocyanomethyl)thio)benzenesulfonamide product was recovered in a yield of 0.7 grams (40 percent of theoretical) and melted at 155°-156° C.
実験手順
To a stirring mixture a 1.5 grams (0.0047 mole) of 3,4,5-trichloro-N,N-dimethyl-2-(mercapto)benzenesulfonamide in 80 milliliters of methanol at 25° C, was added 0.39 grams of sodium methoxide. The mixture was stirred for 15 minutes and thereafter 1.0 gram (0.009 mole) of chloromethylthiocyanate was added thereto and the mixture stirred at room temperature for 3 hours. At the end of this time period, the reaction mixture was filtered to remove the solids which had precipitated. The filtrate further heated at 62° C for 2 hours and after cooling, the solvent was reduced in volume by evaporation under reduced pressure. The solids were thereafter removed by filtration. Additional filtrations gave additional solids. The recovered solids were combined and dissolved in chloroform and filtered. The solvent was removed by evaporation under reduced pressure and the solid product which remained was air dried. The 3,4,5-trichloro-N,N-dimethyl-2-((thiocyanomethyl)thio)benzenesulfonamide product was recovered in a yield of 0.7 grams (40 percent of theoretical) and melted at 155°-156° C.