反応 #2175454
ord-413580587c4f42228161ad2a1f7fdf22
反応方程式
試薬
溶媒
反応条件
後処理
- 1その他In an argon-purged flask
- 2その他was placed in a room temperature
- 3その他The organic solvent was partially removed at reduced pressure
- 4workup.ADDITIONBrine was added
- 5抽出the product was twice extracted with ethyl acetate (300 mL and 100 mL)
- 6洗浄The combined organic layers were washed with brine
- 7乾燥dried over sodium sulfate
- 8ろ過filtered
- 9その他evaporated to dryness
- 10その他The crude product (3.3 g, 83%) was purified by flash chromatography
- 11洗浄silica gel 60 Å eluted with 50:50:2 ethyl acetate/chloroform/glacial acetic acid
実験手順
In an argon-purged flask, crude 9-formyl-7-(3-carboxy-propyl)-4-fluorenecarboxylic acid (4.0 g, 0.0123 mol) was dissolved in anhydrous methanol (50 mL). The flask was placed in a room temperature bath and sodium borohydride (2.3 g, 0.0615 mol) was carefully added to the reaction in portions (Caution! Flammable gas evolution.). The reaction was stirred for two hours and another portion of sodium borohydride was added (1.2 g, 0.031 mol). After another six hours the reaction was treated with a small amount of water. The organic solvent was partially removed at reduced pressure and the mixture was acidified with concentrated HCl. Brine was added and the product was twice extracted with ethyl acetate (300 mL and 100 mL). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and evaporated to dryness. The crude product (3.3 g, 83%) was purified by flash chromatography: silica gel 60 Å eluted with 50:50:2 ethyl acetate/chloroform/glacial acetic acid. The purified product was an orange solid (1.7 g, 43%). 1H-NMR (CD3OD): δ (ppm) 8.3 (d, 1H, Ar); 7.8 (m, 2H, Ar); 7.6 (s, 1H, Ar); 7.4 (t, 1H, Ar); 7.2 (m, 1H, Ar); 4.0 (m, 2H, CH2); 3.9 (m, 1H, CH); 2.8 (t, 2H, CH2); 2.4 (t, 2H, CH2); 2.0 (m, 2H, CH2).