تفاعل #552801
ord-4e266ac6a3bd4c498ad6acbf71707418
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1درجة الحرارةthe mixture is heated
- 2درجة الحرارةat reflux for 48 hours
- 3درجة الحرارةThe reaction mixture is cooled down to 0° C.
- 4workup.STIRRINGThe mixture is stirred at room temperature for 1.5 hour
- 5غسيلThe organic phase is washed with brine (3×30 ml) and saturated sodium sulfite solution (30 ml)
- 6أخرىThe organic phase is dried
- 7ترشيحfiltered
- 8أخرىevaporated
- 9أخرىto give a dark oil which
- 10أخرىis purified by flash chromatography on silica gel using 3:2 ether/hexane as eluent
الإجراء التجريبي
To a solution of methyl 4(S)-allyl-8-(benzyloxy)octanoate (2.4 g, 7.9 mmol) in dry tetrahydrofuran (20 ml) under nitrogen is added a 0.5 M solution of 9-borabicyclononane in tetrahydrofuran (23.6 ml, 11.8 mmol) and the mixture is allowed to stir at room temperature for 18 hours. The reaction mixture is added to a solution of tetrakis-triphenylphosphine palladium (O) (0.13 g, 0.11 mmole as catalyst) and potassium phosphate (5.36 g, 23.3 mmole in tetrahydrofurane (4 ml). Then 3-bromopyridine (1.2 ml, 12.5 mmol) is added and the mixture is heated at reflux for 48 hours. The reaction mixture is cooled down to 0° C. and a 15% solution of sodium hydroxide (8.9 ml) is added followed by hydrogen peroxide (8.9 ml, 30% solution). The mixture is stirred at room temperature for 1.5 hour and then diluted with ether. The organic phase is washed with brine (3×30 ml) and saturated sodium sulfite solution (30 ml). The organic phase is dried, filtered and evaporated to give a dark oil which is purified by flash chromatography on silica gel using 3:2 ether/hexane as eluent to yield methyl 4(R)-[3-(3-pyridyl)propyl]-8-(benzyloxy)octanoate; IR (CH2Cl2): 1732, 1101, 896 cm- 1.