Реакция #1552086
ord-f557c3b5ba314ef1b774ae19baec790e
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1Другоеthe temperature below 37° C
- 2workup.ADDITIONAfter the end of the addition
- 3Другоеis back to room temperature
- 4Другоеthe two phases are separated
- 5Экстракцияthe organic phase is extracted with 100 ml of water
- 6ФильтрацияThe resulting white precipitate is filtered
- 7Промывкаwashed twice with 20 ml of water
- 8Другоеdried
Методика
In a 500 ml flask, 6.0 g (31 mmol) of 5-chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carbaldehyde are added to 30 ml of toluene. A solution of 2.4 g (62 mmol) of sodium hydroxide in 6 ml of water is added to the reaction mixture, followed by 103 ml of a 30% solution of hydrogen peroxide in water, whilst keeping the temperature below 37° C. After the end of the addition, the reaction mixture is stirred at 50° C. for 7 hours. Once the reaction mixture is back to room temperature, the two phases are separated and the organic phase is extracted with 100 ml of water. The combined aqueous phases are acidified to pH 2 with aqueous hydrochloric acid. The resulting white precipitate is filtered, washed twice with 20 ml of water, and dried to yield 3.2 g of 5-chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 3.78 (s, 3H); 7.12 (t, 1H, JHF=53.60 Hz) 13.19 (s, 1H); IR (KBr): 1688 cm−1 (C═O); 2200-3200 cm−1 broad (hydrogen bond).