Hydrochloric Acid → Ethyl 6-chloro-4-hydroxy-3-quinolinecarboxylate

HRID 336864

反応式

HRID 336864 の反応式
[Cl:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.C([O:11][CH:12]=[C:13]([C:19]([O-])=O)[C:14]([O:16][CH2:17][CH3:18])=[O:15])C.Cl.[OH-].[Na+]>C(OCC)(=O)C.O>[CH2:17]([O:16][C:14]([C:13]1[C:12](=[O:11])[C:7]2[C:5](=[CH:4][CH:3]=[C:2]([Cl:1])[CH:8]=2)[NH:6][CH:19]=1)=[O:15])[CH3:18]

参加物

7

実験手順

A mixture of 4-chloroaniline (156.7 mmol) and ethyl ethoxymethylenemalonate (156.7 mmol) was stirred at room temperature until homogeneous. The homogeneous solution was heated in an oil bath at 165° C. for 6 hours. The reaction mixture was cooled to room temperature and 1 N HCl (3 mL) was added. The reaction mixture was stirred and heated to 115° C. for 3 hours. The mixture was cooled to room temperature and then treated with 20 mL of water. The resulting suspension treated with 10 N NaOH solutions to reach the pH about 8. It was partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography using a 9:1 v/v hexane: ethyl acetate as solvent to afford title compound (28 g, 71% yield) as a yellow solid.

後処理

  1. temperatureThe homogeneous solution was heated in an oil bath at 165° C. for 6 hours
  2. temperatureThe reaction mixture was cooled to room temperature
  3. stirringThe reaction mixture was stirred
  4. temperatureheated to 115° C. for 3 hours
  5. temperatureThe mixture was cooled to room temperature
  6. customIt was partitioned between ethyl acetate and water
  7. customThe organic layer was separated
  8. extractionthe aqueous layer was extracted with ethyl acetate
  9. washThe combined organic extracts were washed with brine
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated
  13. customThe crude product was purified by flash column chromatography

出典と根拠

ORDレコード
ord-e6dd59b80fae4a7cafa0105fa0fca600
出典データセット
uspto-grants-2014_11
特許番号
US08889706B2

関連ノート

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