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HRID 1007621생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Pivalic anhydrideHCID 15234—
반응물3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acidHCID 92126—
반응물HCID 178418361HCID 178418361—
촉매Phosphine, tris(4-methylphenyl)-HCID 13956—
촉매palladium(II) acetateHCID 167845—
생성물3-(3-Hydroxy-4-methoxyphenyl)prop-2-enalHCID 5402515749.4%

반응 조건

온도80 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06794531B2
출처 데이터셋uspto-grants-2004_09
ORD IDord-5fbb8291ec95476a9ec895955de679cc
출처 메모uspto-grants-2004_09