Реакция #3342
ord-dc25bdb7c4ad482f819d561626b78d70
Уравнение реакции
Реагенты
Нет
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Экстракцияextracted with 100 mL of chloroform (CHCl3)
- 2СушкаThe CHCl3 layer was dried over MgSO4
- 3Концентрированиеconcentrated in vacuo
- 4ДругоеThe residue was purified by column chromatography (
- 5ДругоеAs a result, 2-(2-pyridylmethylthio) was initially obtained
Методика
Initially, 2.7 g of 2-chloromethylpyridine hydrochloride was added to a solution of 2.4g of 5,5-dimethyl-2,4-dithiohydantoin in 17 mL of 2N aqueous solution of NaOH. The reaction mixture was stirred for one hour at the room temperature, and extracted with 100 mL of chloroform (CHCl3). The CHCl3 layer was dried over MgSO4 and concentrated in vacuo. The residue was purified by column chromatography (using CHCl3 as a developing solvent). As a result, 2-(2-pyridylmethylthio) was initially obtained. From the earlier fractions, the desired compound of 2-(2-pyridylmethylthio)-5,5-dimethylimidazolin-4-thione was isolated in the form of a syrup. The yield of this compound was 1.02 g with a yield ratio of 27.1%.