تفاعل #2487421
ord-b563cb31190f4d76bd2fd008dd292eda
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىdegassed
- 2درجة الحرارةthe mixture is refluxed for 60 h
- 3درجة الحرارةAfter cooling
- 4أخرىthe organic phase is separated off
- 5غسيلwashed three times with 200 ml of water
- 6تجفيفonce with 200 ml of saturated aqueous sodium chloride solution and subsequently dried over magnesium sulfate
- 7ترشيحAfter the desiccant has been filtered off
- 8أخرىthe organic phase is evaporated to dryness under reduced pressure in a rotary evaporator
- 9أخرىThe grey residue obtained in this way
- 10أخرىis recrystallised from dioxane
- 11ترشيحThe deposited crystals are filtered off with suction
- 12غسيلwashed with 50 ml of ethanol
- 13أخرىsubsequently dried under reduced pressure
الإجراء التجريبي
1.78 g (5.6 mmol) of tri-o-tolylphosphine and 0.2 g (0.9 mmol) of palladium acetate are added to a vigorously stirred, degassed suspension of 22.8 g (93.3 mmol) of 4-trimethylsilyinaphth-1-ylboronic acid, 37.4 g (93.3 mmol) of 9-(4-methylnaphth-1-yl)anthracene and 90 g (230 mmol) of tripotassium phosphate in a mixture of 575 ml of water, 100 ml of dioxane and 860 ml of toluene, and the mixture is refluxed for 60 h. After cooling, the organic phase is separated off, washed three times with 200 ml of water and once with 200 ml of saturated aqueous sodium chloride solution and subsequently dried over magnesium sulfate. After the desiccant has been filtered off, the organic phase is evaporated to dryness under reduced pressure in a rotary evaporator. The grey residue obtained in this way is recrystallised from dioxane. The deposited crystals are filtered off with suction, washed with 50 ml of ethanol and subsequently dried under reduced pressure; yield: 38 g, 79% of theory; purity: 99.9% according to HPLC.