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HRID 12613作成日:2026年10月23日

Triethylamine → Ethyl [3-(2,4-dichlorobenzoyl)-2-oxocyclohexyl]acetate

https://huagongshe.com/ja/reaction/12613

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl AcetateHCID 8857—
反応物2,4-Dichlorobenzoyl chlorideHCID 66645—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl [3-(2,4-dichlorobenzoyl)-2-oxocyclohexyl]acetateHCID 86615521—

反応手順

Intermediate 2 (2 g, 8.44 mmol) was dissolved in dioxane (50 ml) and triethylamine (1.18 ml, 8.44 mmol) and 2,4-dichlorobenzoyl chloride (1.76 g, 844 mmol) added. The reaction mixture was stirred at reflux for 16 h. The mixture was then allowed to cool and diluted with ethyl acetate and washed with saturated sodium bicarbonate and then brine. The organics were dried over sodium sulfate and purified by column chromatography to give the desired ethyl [3-(2,4-dichlorobenzoyl)-2-oxocyclohexyl]acetate (220 mg) as a colourless oil. 1H NMR δ (ppm)(CDCl3): 7.36 (1H, d, J=2.0 Hz), 7.23, (1 H, dd, J=8.3, 2.0 Hz), 7.12 (1 H, d, J=8.3 Hz), 4.13-4.07 (2 H, m), 2.93-2.84 (1 H, m), 2.78 (1 H, dd, J=16.1, 5.9 Hz), 2.45 (1 H, dd, J=16.1, 8.3 Hz), 2.11-1.84 (4 H, m), 1.70-1.62 (1 H, m), 1.51-1.40 (2 H, m), 1.20 (3 H, t, J=7.0 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728022B2
出典データセットuspto-grants-2010_06
ORD IDord-e96109b552dd4f269eee287f5bebff85
出典メモuspto-grants-2010_06