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HRID 1007621作成日:2026年10月23日

Pivalic anhydride → 3-(3-Hydroxy-4-methoxyphenyl)prop-2-enal

https://huagongshe.com/ja/reaction/1007621

反応式

関与物質

役割名称HCID仕込み量
反応物Pivalic anhydrideHCID 15234—
反応物3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acidHCID 92126—
反応物HCID 178418361HCID 178418361—
触媒Phosphine, tris(4-methylphenyl)-HCID 13956—
触媒palladium(II) acetateHCID 167845—
生成物3-(3-Hydroxy-4-methoxyphenyl)prop-2-enalHCID 5402515749.4%

反応条件

温度80 °C

反応手順

Palladium acetate (58 mg, 0.257 mmol), tri(p-tolyl) phosphine (157 mg, 0.515 mmol), 3-hydroxy-4-methoxycinnamic acid (5.00 g, 25.7 mmol) and pivalic acid anhydride (14.4 g, 77.2 mmol) were added thereto, and thereafter the mixture was bubbled with nitrogen gas for 30 minutes to substitute nitrogen gas completely for the gas in the system of reaction, whereby the system was filled with nitrogen gas. Next, hydrogen gas was added thereinto to substitute hydrogen gas for the gas in the system, and then the mixture was stirred under hydrogen pressure of 3.4 MPa at 80° C. for 24 hours for reaction. Thus obtained reaction solution was concentrated under reduced pressure to remove tetrahydrofuran by vaporization. The remaining residue was subjected to a purification process with a silica gel column chromatography (eluting solvent: toluene/ethyl acetate=4/1) to obtain 3-hydroxy-4-methoxycinnamaldehyde (2.26 g, 12.7 mmol, yield: 49%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06794531B2
出典データセットuspto-grants-2004_09
ORD IDord-5fbb8291ec95476a9ec895955de679cc
出典メモuspto-grants-2004_09