Реакция #577199
ord-4ca55afa719f4b9788b2d1b692eccdeb
Уравнение реакции
Реагенты
Условия реакции
Обработка
- 1Другоеequipped with a mechanical stirrer
- 2ТемператураThe reaction mixture was heated at 70° C. for 4 hours
- 3ТемператураAfter cooling to room temperature
- 4ЭкстракцияThe aqueous layer was extracted with diethyl ether (1×400 mL)
- 5Другоеto remove the neutral products
- 6ДругоеA brownish-yellow oily solid was obtained from the aqueous layer
- 7Экстракцияwas extracted with 3×300 mL of ethyl acetate
- 8Промывкаwashed with saturated NaCl solution (1×500 mL)
- 9Сушкаdried over anhydrous sodium sulfate
- 10ДругоеRemoval of the solvent
- 11Другоеby rotary evaporation
Методика
Potassium t-butoxide (68.8 g) was weighed into a reaction flask equipped with a mechanical stirrer, placed under a nitrogen atmosphere and 700 mL of toluene was added followed by 4,4′-difluorobenzophenone (100 g). The reaction mixture was stirred mechanically and heated to 70° C. A solution of dimethyl succinate (80 g) in 100 mL of toluene was added to the reaction mixture over a 60 minute period. The reaction mixture was heated at 70° C. for 4 hours. After cooling to room temperature, the reaction mixture was poured into 500 mL of water and the toluene layer discarded. The aqueous layer was extracted with diethyl ether (1×400 mL) to remove the neutral products, and then acidified the aqueous layer with concentrated HCl. A brownish-yellow oily solid was obtained from the aqueous layer, and was extracted with 3×300 mL of ethyl acetate. The organic layers were combined, washed with saturated NaCl solution (1×500 mL) and dried over anhydrous sodium sulfate. Removal of the solvent by rotary evaporation yielded 122 g of 4,4-di(4-fluorophenyl))-3-methoxycarbonyl-3-butenoic acid as a brownish oily solid. This material was not purified further but was used directly in the next step.