تفاعل #470385
ord-abc8b06cfe5c4a7aa2d98e0b2bc37d7c
معادلة التفاعل
ظروف التفاعل
المعالجة
- 1workup.ADDITIONwere added
- 2استخلاصthe mixture was subject to extraction
- 3استخلاصThen, an organic layer extracted
- 4أخرىtherefrom was dried
- 5ترشيحfiltered
- 6أخرىA solvent was removed
- 7أخرىthe resultant was separated
الإجراء التجريبي
1.11 g (4.7 mmol) of 3,5-dibromo-pyridin, 1.0 g (3.92 mmol) of 3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-quinoline, 0.45 g of tetrakis(triphenylphosphine)palladium(0), 7.84 ml of 2 M K2CO3 and 1.26 g of tetrabutylammoniumbromide were added to a 100 ml round-bottom flask in an argon atmosphere, and 30 ml of THF and 15 ml of toluene were added thereto. Then, the mixture was refluxed at 100° C. for 16 hours. When the mixture solution turned dark brown, water was added thereto and the mixture was subject to extraction using chloroform. Then, an organic layer extracted therefrom was dried using anhydrous magnesium sulfate and filtered. A solvent was removed and the resultant was separated using a silica gel column chromatography to obtain 1.1 g of white solid 3-(5-bromo-pyridin-3-yl)-quinoline which was identified by an atmospheric pressure chemical ionization (APCI) using LCMS (SHIMADZU, LCMS-IT-TOF). As a result, a main peak was observed at [M+H]+=285.