反应 #2460293
ord-f3ebc37c1fde41a3a684bcc72fb02e82
反应方程式
2-(4-butoxyphenoxy)benzoic acid
sulfuric acid
→
2-butoxyxanthen-9-one
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度The mixture was cooled to ambient, and
- 2其他The precipitated crude product
- 3其他was collected
- 4洗涤washed with water, and air
- 5其他dried
- 6其他The product was purified by column chromatography
- 7其他followed by recrystallization from 50% aqueous ethanol
- 8其他A white powder was obtained
实验过程
Finally, 2-butoxyxanthen-9-one (S-14) was synthesized. A stirred suspension under argon of 2-(4-butoxyphenoxy)benzoic acid (8.2 g, 29 mmol) in acetic anhydride (50 mL) was treated with 2.8 g (29 mmol) of concentrated sulfuric acid, and then held at 80° C. for 3 h. The mixture was cooled to ambient, and then poured onto 500 g of ice. The precipitated crude product was collected, washed with water, and air dried. The product was purified by column chromatography followed by recrystallization from 50% aqueous ethanol. A white powder was obtained. 1H NMR (CDCl3): δ 1.00 (t, 3H), 1.5 (m, 2H), 1.85 (m, 2H), 4.08 (t, 2H), 7.3-7.5 (m, 4H), 7.7 (m, 2H), 8.36 (d, 1H).