تفاعل #1483118
ord-2d144cb8cdd9424f82e12bf934b63356
معادلة التفاعل
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةAt the end of this period the reaction was cooled
- 2غسيلThe organic layer was washed with water (3×100 mL) and intermittently with brine
- 3أخرىformed
- 4ترشيحThe organic layer was filtered through a pad of celite
- 5تجفيفdried over MgSO4
- 6ترشيحfiltered
- 7تركيزconcentrated to an oil
- 8workup.DISSOLUTIONThe oil was dissolved in CH2Cl2 (20 mL)
- 9workup.ADDITIONdiethyl ether (150 mL) added
- 10workup.ADDITIONWith good stirring, a 20% solution of concentrated HCl in ethanol (20 mL) was added
- 11ترشيحThe yellow 2-(2-methoxyphenyl)-1,10-phenanthroline hydrochloride chloride was filtered off
- 12غسيلwashed with ether
- 13أخرىair-dried
الإجراء التجريبي
2-Chloro-1,10-phenanthroline (5.9 g, 27.5 mMole), 2-methoxyphenylboronic acid (2) (5 g, 33 mMole), tetrakis(triphenylphosphine)palladium(0) (1 g, 0.825 mMole), 2M-Na2CO3 (33 mL, 66 mMole) and ethanol (8 mL) were suspended in toluene (70 mL) and heated to 100° C. with good stirring for 24 hours. At the end of this period the reaction was cooled, diluted with ethyl acetate (200 mL) and the aqueous layer run off. The organic layer was washed with water (3×100 mL) and intermittently with brine to break up any emulsion formed. The organic layer was filtered through a pad of celite, dried over MgSO4, filtered and concentrated to an oil. The oil was dissolved in CH2Cl2 (20 mL) and diethyl ether (150 mL) added. With good stirring, a 20% solution of concentrated HCl in ethanol (20 mL) was added. The yellow 2-(2-methoxyphenyl)-1,10-phenanthroline hydrochloride chloride was filtered off, washed with ether and air-dried. Yield 9.7 g.