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HRID 336864作成日:2026年10月26日

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

https://huagongshe.com/reaction/336864

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-ChloroanilineHCID 7812—
反応物Sodium HydroxideHCID 14798—
反応物3-Ethoxy-2-ethoxycarbonylprop-2-enoateHCID 85829211—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 6-chloro-4-hydroxy-3-quinolinecarboxylateHCID 71811371%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889706B2
出典データセットuspto-grants-2014_11
ORD IDord-e6dd59b80fae4a7cafa0105fa0fca600
出典メモuspto-grants-2014_11