Реакция #65524
ord-3205d55d0545420eb710b79417a1f784
Уравнение реакции
Реагенты
Условия реакции
Обработка
- 1Температураchilled to ≤-50° C. in a dry ice/acetone bath
- 2workup.ADDITIONwas slowly added
- 3Температураto warm to room temperature
- 4Другоеthe solvent was removed under reduced pressure
- 5Фильтрацияfiltered
- 6Промывкаwashed with water (500 mL)
- 7ПромывкаIt was then washed throughly with ethanol (1.5 L)
- 8Фильтрацияfiltered
- 9Другоеdried
Методика
To a batch of 1-lithiophenoxathiin 10,10-dioxide, prepared according to the procedure of Example 1B from 44 g of phenoxathiin 10,10-dioxide chilled to ≤-50° C. in a dry ice/acetone bath, was slowly added chilled acetaldehyde (20.37 g). The reaction mixture was maintained at -50° C. during the addition which took 45 min. It was then allowed to warm to room temperature, and the solvent was removed under reduced pressure. The yellow-orange residue was stirred overnight with 0.5 N hydrochloric acid (259 mL), filtered and washed with water (500 mL). It was then washed throughly with ethanol (1.5 L), filtered and dried to give 1-(1-hydroxyethyl) phenoxathiin 10,10-dioxide (41 g) which was sufficiently pure for the next step (conversion to 1-ethylphenoxathiin 10,10-dioxide).