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HRID 428714作成日:2026年10月27日

Methyl 4-Formylbenzoate → Methyl 4-ethenylbenzoate

https://huagongshe.com/reaction/428714

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-FormylbenzoateHCID 15294—
反応物ButyllithiumHCID 178418339—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒Diethyl EtherHCID 3283—
生成物Methyl 4-ethenylbenzoateHCID 583124—

反応手順

To a stirred solution of n-butyllithium (4 mL, 2,5 M solution in hexane, 10 mmol) (Aldrich) in ether (30 mL) was added methyltriphenylphosphonium bromide (3.57 g, 10 mmol) (Aldrich) over a period of 5 min. The reaction mixture was stirred for 4 h at room temperature. To the resulting orange solution was added methyl 4-formylbenzoate (1.54 mL, 10 mmol) dropwise. The solution became colorless, and a white precipitate separated. The mixture was then heated to reflux and immediately allowed to cool to room temperature. The precipitate was removed by filtration. The resulting precipitate was washed with ether, and the combined ethereal filtrates were washed with water until neutral and then dried over anhydrous MgSO4. The solvent was removed and the residue, 4-ethenyl-benzoic acid methyl ester, was used in the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313310B1
出典データセットuspto-grants-2001_11
ORD IDord-8693104f274b45b6a1977f38b376508b
出典メモuspto-grants-2001_11