反应 #2460293

ord-f3ebc37c1fde41a3a684bcc72fb02e82

反应方程式

CCCCOc1ccc(Oc2ccccc2C(=O)O)cc1
2-(4-butoxyphenoxy)benzoic acid
O=S(=O)(O)O
sulfuric acid
CCCCOc1ccc2oc3ccccc3c(=O)c2c1
2-butoxyxanthen-9-one

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The mixture was cooled to ambient, and
  2. 2
    其他The precipitated crude product
  3. 3
    其他was collected
  4. 4
    洗涤washed with water, and air
  5. 5
    其他dried
  6. 6
    其他The product was purified by column chromatography
  7. 7
    其他followed by recrystallization from 50% aqueous ethanol
  8. 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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07459263B2uspto-grants-2008_12