Pyridine → Ethyl 3-oxo-4-phenylbutanoate

HRID 514332

反応式

HRID 514332 の反応式
[C:1]1([CH2:7][C:8](Cl)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:11][C:12]1(C)[O:17]C(=O)[CH2:15][C:14](=O)[O:13]1.N1C=CC=CC=1>C(Cl)Cl>[O:9]=[C:8]([CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[CH2:11][C:12]([O:13][CH2:14][CH3:15])=[O:17]

参加物

5

反応条件

温度
0 °C

実験手順

To a solution of phenylacetyl chloride (1 mL, 7.56 mmol) was added dropwise a solution of 2,2-dimethyl-1,3-dioxane-4,6-dione (1.09 g, 7.56 mmol) and pyridine (1.3 mL) in CH2Cl2 (20 mL) at 0° C. The solution was stirred for 30 min at 0° C., then allowed to warm slowly to rt and stirred overnight. The reaction mixture was then washed with 10% aqueous HCl (2×10 mL). The organic layer was dried (MgSO4), filtered, and concentrated under reduced pressure. The crude residue was dissolved in EtOH (20 mL) and heated under reflux conditions for 4 h. The mixture was cooled to rt and then concentrated under reduced pressure. The resulting oil was purified by flash column chromatography (PE/EA=1/4) to afford the title compound (600 mg, 38%) as a yellow oil. [M+H] Calc'd for C12H14O3, 207. Found, 207.

後処理

  1. temperatureto warm slowly to rt
  2. stirringstirred overnight
  3. washThe reaction mixture was then washed with 10% aqueous HCl (2×10 mL)
  4. dry with materialThe organic layer was dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. dissolutionThe crude residue was dissolved in EtOH (20 mL)
  8. temperatureheated under reflux conditions for 4 h
  9. temperatureThe mixture was cooled to rt
  10. concentrationconcentrated under reduced pressure
  11. customThe resulting oil was purified by flash column chromatography (PE/EA=1/4)

出典と根拠

ORDレコード
ord-1b03c57aae8346dda6683703d537ade2
出典データセット
uspto-grants-2015_08
特許番号
US09107916B2

関連ノート

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