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HRID 1007624作成日:2026年10月27日

Triphenylphosphine → 3-(3-Hydroxy-4-methoxyphenyl)propanal

https://huagongshe.com/reaction/1007624

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物Pivalic anhydrideHCID 15234—
反応物3-Hydroxy-4-methoxybenzenepropanoic acidHCID 2752054—
反応物HCID 178418361HCID 178418361—
触媒palladium(II) acetateHCID 167845—
溶媒TetrahydrofuranHCID 8028—
生成物3-(3-Hydroxy-4-methoxyphenyl)propanalHCID 981540748.3%

反応条件

温度80 °C

反応手順

Into a chemical reactor for hydrogen addition (hydrogenation) under elevated pressure, 3-(3-hydroxy-4-methoxyphenyl) propionic acid (5.09 g, 25.9 mmol), pivalic acid anhydride (14.3 g, 76.6 mmol), and tetrahydrofuran (64 ml) were added, and thereafter the mixture was bubbled with nitrogen gas for 10 minutes. Palladium acetate (57 mg, 0.254 mmol) and triphenylphosphine (349 mg, 1.33 mmol) were added thereto, and thereafter the mixture was bubbled with nitrogen gas for 20 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 5.4 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: hexane/ethyl acetate=2/1). The thus eluted fractions containing the object compound were concentrated under reduced pressure to obtain crude 3-(3-hydroxy-4-methoxyphenyl) propionaldehyde (2.26 g, 12.5 mmol, yield: 48%) in the slightly yellow coloured solid.

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-dd92e597e4f44b2c8659e4a504ec2880
出典メモuspto-grants-2004_09