تفاعل #58985
ord-88340d42c4b64b29a8c104fdb5ee4786
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
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المعالجة
- 1استخلاصthe mixture was extracted with ethyl acetate
- 2تركيزThe ethyl acetate layer was concentrated
- 3workup.ADDITIONa 6N aqueous hydrochloric acid solution (3 ml) and acetic acid (3 ml) were added to the residue
- 4workup.STIRRINGThe mixture was stirred for 3 hrs
- 5درجة الحرارةwith heating
- 6درجة الحرارةunder reflux
- 7تركيزThe reaction mixture was concentrated
- 8workup.ADDITIONpoured into water
- 9ترشيحThe precipitated solids were collected by filtration
- 10غسيلwashed with water
- 11أخرىdried
الإجراء التجريبي
A mixture of 4-(4-fluorophenyl)-1,2,3-thiadiazole-5-carbaldehyde (180 mg), ethyl diethylphosphonoacetate (450 mg), sodium hydride (60% in oil, 40 mg) and N,N-dimethylformamide (3 ml) was stirred at room temperature for 2 hrs. The reaction mixture was poured into a 1N aqueous hydrochloric acid solution and the mixture was extracted with ethyl acetate. The ethyl acetate layer was concentrated, and a 6N aqueous hydrochloric acid solution (3 ml) and acetic acid (3 ml) were added to the residue. The mixture was stirred for 3 hrs. with heating under reflux. The reaction mixture was concentrated and poured into water. The precipitated solids were collected by filtration, washed with water and dried to give (2E)-3-[4-(4-fluorophenyl)-1,2,3-thiadiazol-5-yl]acrylic acid (130 mg, yield 60%) as a pale-yellow solid.