참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pivalic anhydride | HCID 15234 | — |
| 반응물 | 3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acid | HCID 92126 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | Phosphine, tris(4-methylphenyl)- | HCID 13956 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 생성물 | 3-(3-Hydroxy-4-methoxyphenyl)prop-2-enal | HCID 54025157 | 49.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06794531B2 |
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| 출처 데이터셋 | uspto-grants-2004_09 |
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| ORD ID | ord-5fbb8291ec95476a9ec895955de679cc |
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| 출처 메모 | uspto-grants-2004_09 |
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