Реакция #55501
ord-d34113bcc99e43e198cce663f85dd86d
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ТемператураThe mixture is then cooled to 6°-8° C. and, at this temperature, there
- 2workup.ADDITIONare added dropwise within the course of 40 minutes 175 ml
- 3workup.ADDITIONAfter completion of the addition
- 4workup.STIRRINGthe mixture is stirred at 6°-8° C. for a further 30 minutes
- 5workup.WAITThe mixture is then left
- 6Температураto warm up to room temperature
- 7workup.STIRRINGstirred at this temperature for 3 hours
- 8workup.WAITthe mixture is left
- 9workup.STIRRINGto stir for 1 hour
- 10workup.WAITleft
- 11ФильтрацияThe separated precipitate is filtered off
- 12Промывкаback-washed with 200 ml
- 13Сушкаof petroleum ether and dried under reduced pressure, there
Методика
144.5 g. of 2,4-diamino-6-chloropyrimidine are suspended in 2000 ml. of ethanol. While stirring, the suspension is warmed to 35° C. (about 15 minutes), the greater part of the substance passing into solution. The mixture is then cooled to 6°-8° C. and, at this temperature, there are added dropwise within the course of 40 minutes 175 ml. of 40% peracetic acid in glacial acetic acid. After completion of the addition, the mixture is stirred at 6°-8° C. for a further 30 minutes. The mixture is then left to warm up to room temperature and stirred at this temperature for 3 hours. 2000 Ml. of petroleum ether are then added, the mixture is left to stir for 1 hour and then left to stand overnight. The separated precipitate is filtered off, back-washed with 200 ml. of petroleum ether and dried under reduced pressure, there being obtained 2,4-diamino-6-chloropyrimidine-3-oxide. Recrystallization yields analytically-pure product having a melting point of 193° C.