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HRID 860412作成日:2026年10月24日

Hydrochloric Acid → Ethyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoate

https://huagongshe.com/ja/reaction/860412

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-Fluorobenzoyl chlorideHCID 67879—
反応物Ethyl 3-oxo-4-phenylbutanoateHCID 225855—
反応物Magnesium ChlorideHCID 5360315—
溶媒PyridineHCID 1049—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoateHCID 5744452567.5%

反応条件

温度0 °C

反応手順

To a suspensin of magnesium chloride (1.46 g) in tetrahydrofuran (10 ml) was added a solution of ethyl 3-oxo-4-phenylbutanoate (2.0 g) in tetrahydrofuran (10 ml) and the mixture was cooled to 0° C., then pyridine (2.5 ml) was added. The mixture was stirred at 20° C. for 30 minutes, then a solution of 4-fluorobenzoyl chloride (2.44 g) in tetrahydrofuran (10 ml) was added at 0° C. After stirring at 20° C. for 2 hours, the mixure was partitoned between 0.5N hydrochloric acid and ethyl acetate. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:5) to give ethyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoate (2.15 g) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07153854B2
出典データセットuspto-grants-2006_12
ORD IDord-6e2cc6132f9e4460b2e12f9e04928393
出典メモuspto-grants-2006_12