Реакция #56445
ord-4fe72f7d2c974fcd9f4fea9ce41b54ae
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.ADDITIONare added
- 2Другоеis 20° C. at the start
- 3Другоеsolution of the precipitate formed
- 4ТемператураThe mixture is cooled
- 5Фильтрацияthe p-chlorobenzylsulphinyl-acetohydroxamic acid is filtered off
- 6ДругоеThis acid is recrystallised from acetic acid
- 7Фильтрацияfiltered off
- 8Промывкаthe precipitate is washed with water and with ethanol
- 9Другоеdried
- 10Другое31.9 g of CRL 40,411 are collected
Методика
31.7 g (0.091 mol) of p-chlorobenzylmercaptoacetohydroxamic acid are mixed with 100 ml of anhydrous acetic acid and 9.1 ml of hydrogen peroxide of 110 volumes strength are added. The temperature, which is 20° C. at the start, rises and solution of the precipitate formed is also observed. The temperature is maintained at 50° C. and after several minutes it is found that the sulphinyl derivative sets solid. 50 ml of acetic acid are now added and the temperature is kept at 50° C. for 1 hour whilst stirring vigorously. The mixture is cooled and the p-chlorobenzylsulphinyl-acetohydroxamic acid is filtered off. This acid is recrystallised from acetic acid and filtered off, the precipitate is washed with water and with ethanol, and dried, and 31.9 g of CRL 40,411 are collected. Yield 85%; instantaneous melting point 210° C. (with decomposition).