反应 #155323

ord-bd794614aa9f415481ca693716300b61

反应方程式

c1ccccc1
benzene
CCCOc1cc2ccccc2cc1N
3-propoxynaphthalen-2-ylamine
CCOC(=O)C(C(C)=O)c1ccc(OC)cc1
ethyl α-acetyl-4-methoxyphenylacetate
CCOC(C)=O
Ethyl acetate
CCCOc1cc2ccccc2c2c(=O)c(-c3ccc(OC)cc3)c(C)[nH]c12
2-(4-methoxyphenyl)-3-methyl-5-propoxy-4H-benzo[f]quinolin-1-one
收率 72.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added 85 mg of Amberlyst 15 (Sigma-Aldrich)
  2. 2
    温度The resulting mixture was heated
  3. 3
    温度under reflux for 20 hours
  4. 4
    过滤filtered
  5. 5
    其他to remove resin
  6. 6
    浓缩the filtrate was concentrated under reduced pressure
  7. 7
    workup.ADDITIONDiphenyl ether (2.8 ml) was added to the residue
  8. 8
    温度the mixture was then heated with a mantle heater
  9. 9
    温度under reflux
  10. 10
    其他The resulting reaction mixture
  11. 11
    温度was cooled to room temperature
  12. 12
    其他directly purified
  13. 13
    浓缩The purified product was concentrated under reduced pressure
  14. 14
    其他giving an oily substance (800 mg, yield: 72%)
  15. 15
    其他to crystallize
  16. 16
    其他recrystallized from ethyl acetate

实验过程

To a benzene solution (38 ml) containing 3-propoxynaphthalen-2-ylamine (600 mg, 2.98 mmol) and ethyl α-acetyl-4-methoxyphenylacetate (1.41 g, 5.96 mmol) was added 85 mg of Amberlyst 15 (Sigma-Aldrich). The resulting mixture was heated under reflux for 20 hours using a Dean-Stark trap. The reaction mixture was cooled to room temperature, filtered to remove resin, and then the filtrate was concentrated under reduced pressure. Diphenyl ether (2.8 ml) was added to the residue, and the mixture was then heated with a mantle heater and stirred for 70 minutes under reflux. The resulting reaction mixture was cooled to room temperature, and then directly purified using silica gel column chromatography (dichloromethane:methanol=80:1→70:1). The purified product was concentrated under reduced pressure, giving an oily substance (800 mg, yield: 72%). Ethyl acetate and n-hexane were added to the thus-obtained oily substance to crystallize and then recrystallized from ethyl acetate, giving a pale yellow powder of 2-(4-methoxyphenyl)-3-methyl-5-propoxy-4H-benzo[f]quinolin-1-one (290 mg).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE045108E1uspto-grants-2014_09