تفاعل #362362
ord-8f2f5c3673ad4efa8cb9b7e67959ba04
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةto warm to room temperature
- 2workup.ADDITIONwas poured into a separatory funnel
- 3workup.STIRRINGThe layers were agitated
- 4أخرىseparated
- 5غسيلthe organic layer was washed with saturated sodium chloride solution
- 6تجفيفdried over anhydrous magnesium sulfate
- 7ترشيحfiltered
- 8تركيزconcentrated
- 9أخرىThe crude product was purified by column chromatography on silica gel (elution with 1:1 methylene chloride/hexanes)
الإجراء التجريبي
A solution of 2-adamantyl-5-iodoanisole (1.29 g, 3.51 mmol) in anhydrous THF (50 mL) was cooled to -78° C. under argon and treated with t-butyllithium solution (4.34 mL, 1.7 M in pentane, 7.37 mmol). The reaction mixture was stirred at -78° C. for 20 min. and then treated with anhydrous N,N-dimethylformamide (0.28 g, 3.86 mmol). The reaction mixture was allowed to warm to room temperature, and was poured into a separatory funnel containing diethyl ether and saturated ammonium chloride solution. The layers were agitated and separated, and the organic layer was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude product was purified by column chromatography on silica gel (elution with 1:1 methylene chloride/hexanes) to afford 0.38 g (43% yield) of 4-(1-Adamantyl)-3-methoxybenzaldehyde as a white solid; 1H NMR (300 MHz, CDCl3) δ 9.92 (s, 1H, CHO), 7.37 (m, 3H, ArH), 3.88 (s, 3H, OCH3), 2.08 (s, 9H, adamantyl), and 1.76 (s, 6H, adamantyl); 13C NMR (75 MHz, CDCl3) δ 192.04 (C=O), 159.38, 146.00, 135.36, 127.06, 124.45, 109.54, 55.09 (OCH3), 40.15, 37.79, 36.95, and 28.90; IR (KBr) 2965, 2900, 2850, 1690 (C=O), 1250, 1160, 1135, 1035, and 1025 cm-1 ; MS (DCI) m/e 271 (MH+), 135 (C10H15+) . Anal. Calcd for C18H22O2.0.015 H2O: C, 79.88; H, 8.21. Found: C, 79.48; H, 8.34.