تفاعل #53556
ord-109991864653475a9fb514957c60a928
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىThe resulting reaction mixture
- 2استخلاصthe organic matters were extracted with 20 ml of ethyl acetate twice
- 3غسيلwashed with 30 ml of water twice
- 4تجفيفdried over anhydrous magnesium sulfate
- 5workup.DISTILLATIONthe ethyl acetate was distilled off under reduced pressure
- 6أخرىPurification of the residue by silica gel column chromatography
الإجراء التجريبي
0.9 g (3.3 mmol) of 2-mercapto-4-(3-trifluoromethylpyrazolyl)benzonitrile, 0.5 g (3.3 mmol) of cyclobutylmethyl bromide and 0.55 g (4.0 mmol) of potassium carbonate were stirred in 5 ml of N,N-dimethylformamide at room temperature overnight. The resulting reaction mixture was poured into 50 ml of water and the organic matters were extracted with 20 ml of ethyl acetate twice. The ethyl acetate layers were combined, then washed with 30 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 0.24 g of 2-cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile (yield 21.2%) as a pale yellow powder (m.p. 102-103° C.).