تفاعل #68758
ord-f9debeb7e7ec4267bfd5613e8c24221f
معادلة التفاعل
المتفاعلات
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىAfter evacuating
- 2أخرىflushing with nitrogen (×3) the mixture
- 3استخلاصAfter dilution with distilled water the crude product is extracted with ethyl acetate (×3)
- 4غسيلthe organic phase is washed with brine
- 5تجفيفdried over magnesium sulfate
- 6تركيزconcentrated in vacuo
- 7أخرىThe crude product is then purified by flash column chromatography on silica gel (isohexane/ethyl acetate eluant)
- 8أخرىfurther triturated with hexanes
الإجراء التجريبي
To a mixture of 2-(5-bromo-2-cyclopropylphenyl)cyclopentane-1,3-dione (0.100 g, 0.34 mmol), 2,4-dichlorophenylboronic acid (0.090 g, 0.47 mmol), [1,1′-bis(diphenylphosphino)-ferrocene]palladium(II)chloride (22 mg, 0.027 mmol) and cesium fluoride (0.152 g, 1.0 mmol) is added 1,2-dimethoxyethane (1 ml). After evacuating and flushing with nitrogen (×3) the mixture is heated at 160° C. for 15 minutes under microwave irradiation. After dilution with distilled water the crude product is extracted with ethyl acetate (×3), and the organic phase is washed with brine, dried over magnesium sulfate and concentrated in vacuo. The crude product is then purified by flash column chromatography on silica gel (isohexane/ethyl acetate eluant) and further triturated with hexanes to afford 2-(2′,4′-dichloro-4-cyclopropylbiphenyl-3-yl)-cyclopentane-1,3-dione as a white powder.