関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Glycine methyl ester hydrochloride | HCID 122755 | — |
| 反応物 | Methyl 2,4-dimethoxy-beta-oxobenzenepropanoate | HCID 2063901 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (Z)-Methyl 3-(2,4-dimethoxyphenyl)-3-((2-ethoxy-2-oxoethyl)amino)acrylate | HCID 86684695 | 69.2% |
反応手順
To a solution of methyl 3-(2,4-dimethoxyphenyl)-3-oxopropanoate (5.0 g, 21 mmol) in EtOH (30 mL) was added glycine methyl ester hydrochloride (10.5 g, 83.9 mmol) followed by acetic acid (1.20 mL, 21 mmol) and triethylamine (8.5 g, 83.9 mmol) and the reaction mixture was heated at 100° C. for 18 hours. After cooling to room temperature, the residue was partitioned between EtOAc and saturated aqueous ammonium chloride. The organic layer was washed with brine, dried over sodium sulfate and concentrated in vacuo. The crude product was dissolved in CH2Cl2 (10 mL) filtered through a plug of silica gel, eluting with 15-35% EtOAc in heptanes and dried under vacuum to give the title compound (4.7 g, 69%) as a yellow solid. This material was used in the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08835449B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-9921a0d60d1748beb999e57d661a0712 |
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| 出典メモ | uspto-grants-2014_09 |
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