تفاعل #169512
ord-c1b632a1a748412dbe54abf3a9082c1a
معادلة التفاعل
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىThe solvent ethanol was then removed under a reduced pressure
- 2أخرىThe two phases were separated
- 3تجفيفthe organic layer was dried over anhydrous Na2SO4
- 4ترشيحfiltered
- 5تركيزconcentrated
- 6أخرىThe residue was purified on silica gel using 5 percent EtOAc in hexane
الإجراء التجريبي
A solution of 5-(1-bromoethyl)-2-(trichloromethyl)pyridine (A) (0.95 g, 3.14 mmol) in ethanol (15 mL) was treated with sodium thiomethoxide (0.44 g, 6.29 mmol) portionwise at 0° C. The mixture was stirred at room temperature overnight. The solvent ethanol was then removed under a reduced pressure and the residue was re-taken into CH2Cl2 and brine. The two phases were separated and the organic layer was dried over anhydrous Na2SO4, filtered, concentrated. The residue was purified on silica gel using 5 percent EtOAc in hexane to give 0.57 g of the partially pure 5-[1-(methylthio)ethyl]-2-(trichloromethyl)pyridine (B) in 67 percent crude yield. GC-MS: mass calcd for C9H10Cl3NS [M]+ 269. Found 269.