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HRID 1372607作成日:2026年10月26日

Ethanol → Ethyl 2-(3-fluoro-4-nitrophenyl)acetate

https://huagongshe.com/reaction/1372607

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sulfuric AcidHCID 1118—
反応物Trifluoroacetic acidHCID 6422—
反応物Di-tert-butyl (3-fluoro-4-nitrophenyl)malonateHCID 67407431—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 2-(3-fluoro-4-nitrophenyl)acetateHCID 1785952996.3%

反応手順

Trifluoroacetic acid (25 ml) was added to a solution of di-tert-butyl (3-fluoro-4-nitrophenyl)malonate (5.11 g, 14.4 mmol) in methylene chloride (50 ml). The resulting mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure to yield a colorless solid substance. To the solid substance were added concentrated sulfuric acid (1 ml) and ethanol (50 ml) and the mixture was heated and refluxed for 2 hours. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. Ice water (100 ml) was poured in the residue, followed by extraction with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium bicarbonate, dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent, whereby ethyl 3-fluoro-4-nitrophenylacetate (3.15 g, 96%) was obtained as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07157487B2
出典データセットuspto-grants-2007_01
ORD IDord-7ec54c886a5044ea8652c2fa05073b38
出典メモuspto-grants-2007_01