반응 #2175454
ord-413580587c4f42228161ad2a1f7fdf22
반응 방정식
시약
용매
반응 조건
후처리
- 1기타In an argon-purged flask
- 2기타was placed in a room temperature
- 3기타The organic solvent was partially removed at reduced pressure
- 4workup.ADDITIONBrine was added
- 5추출the product was twice extracted with ethyl acetate (300 mL and 100 mL)
- 6세척The combined organic layers were washed with brine
- 7건조dried over sodium sulfate
- 8여과filtered
- 9기타evaporated to dryness
- 10기타The crude product (3.3 g, 83%) was purified by flash chromatography
- 11세척silica gel 60 Å eluted with 50:50:2 ethyl acetate/chloroform/glacial acetic acid
실험 절차
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).