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HRID 225951作成日:2026年10月26日

Water → Ethyl 3-(benzothiophen-2-yl)-5-ethyl-4,5-dihydro-5-isoxazolecarboxylate

https://huagongshe.com/reaction/225951

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl 2-methylidenebutanoateHCID 291416—
反応物Sodium HypochloriteHCID 23665760—
反応物Benzothiophen-2-aldehyde oximeHCID 85255485—
触媒TriethylamineHCID 8471—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-(benzothiophen-2-yl)-5-ethyl-4,5-dihydro-5-isoxazolecarboxylateHCID 6882966018%

反応手順

Benzothiophen-2-aldehyde oxime derivative (400 mg, 2.26 mmol) prepared according to the same procedure as Preparation 1 was dissolved in THF (25 ml), and the mixture was kept at 0□. Ethyl 2-ethylacrylate (434 mg, 1.5 Eq) and triethylamine (7 drops) were dissolved in THF (5 ml), thus obtained solution was slowly added to the above, and sodium hypochlorite solution (6.0 ml) was further added. The reaction solution was warmed to room temperature and stirred for 4 hours. Water (20 ml) was added, and the mixture was extracted with ethyl acetate (40 ml×2), washed with aqueous sodium chloride solution (20 ml), dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography (20% ethyl acetate-hexane) to give the title compound (121 mg, Yield 18%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557133B2
出典データセットuspto-grants-2009_07
ORD IDord-e2fa1e311a79428eb715b292d4618aea
出典メモuspto-grants-2009_07