関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pivalic anhydride | HCID 15234 | — |
| 反応物 | 3-(3-Hydroxy-4-methoxyphenyl)prop-2-enoic acid | HCID 92126 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Phosphine, tris(4-methylphenyl)- | HCID 13956 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 生成物 | 3-(3-Hydroxy-4-methoxyphenyl)prop-2-enal | HCID 54025157 | 49.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06794531B2 |
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| 出典データセット | uspto-grants-2004_09 |
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| ORD ID | ord-5fbb8291ec95476a9ec895955de679cc |
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| 出典メモ | uspto-grants-2004_09 |
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