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HRID 28554作成日:2026年10月23日

Hydrochloric Acid → Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate

https://huagongshe.com/ja/reaction/28554

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TriethylamineHCID 8471—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物Magnesium ChlorideHCID 5360315—
反応物NatriummalonesterHCID 23662308—
反応物(5-Chloro-2-methoxy-phenyl)-imidazol-1-yl-methanoneHCID 68987646—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoateHCID 5401234776%

反応条件

温度10 °C

反応手順

To a stirred mixture of ethyl malonate sodium salt (3.8 g, 24.7 mmol) and magnesium sulfate (3.2 g, 26.3 mmol) in acetonitrile (60 ml) was added triethylamine (4.7 ml, 33.5 mmol) under an argon atmosphere. After stirring for 2 hours, the solution containing (5-chloro-2-methoxy-phenyl)-imidazol-1-yl-methanone was added. After stirring at 80° C. for 2 hours, magnesium chloride (2.5 g, 26.3 mmol) was added and the mixture was stirred for 16 hours. After cooling to 10° C., concentrated hydrochloric acid (5 ml) was added and the mixture was stirred for 30 minutes. The layers were separated and the aqueous layer was extracted with ethyl acetate (3×60 ml). The combined organic layers were dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:4 followed by 1:3) to provide 3-(5-chloro-2-methoxy-phenyl)-3-oxopropionic acid ethyl ester (2.3 g, 76% yield) as an oil. 1H NMR (CDCl3) δ 1.23 (t, 3H, J=8.7 Hz CH3), 3.89 (s, 3H, CH3), 3.94 (s, 2H, CH2), 4.17 (q, 2H, CH2), 6.91 (d, 1H, J=8.6 Hz, Ar), 7.45 (dd, 1H, J=8.8 Hz, J=2.6 Hz, Ar), 7.85 (d, 1H, J=2.6 Hz, Ar).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419984B2
出典データセットuspto-grants-2008_09
ORD IDord-bdb4a6607416413d9cebb779de9ff903
出典メモuspto-grants-2008_09