関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl cyanoacetate | HCID 7764 | — |
| 反応物 | 3-Methylacetophenone | HCID 11455 | — |
| 反応物 | Ammonium Acetate | HCID 517165 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2-Cyano-3-(3-methylphenyl)-but-2-enoic acid ethyl ester | HCID 297786 | — |
反応手順
A mixture of 3′-methylacetophenone (50 mmol), ethyl cyanoacetate (50 mmol), 25 acetic acid (1.14 mL) ammonium acetate (400 mg), and benzene (50 mL) was heated to reflux in a Dean-Stark apparatus. After approximately 10 hours, additional ethyl cyanoacetate (50 mmol), acetic acid (1.14 mL), and ammonium acetate (400 mg) are added. After an additional 10 hours, the reaction was cooled to room temperature, diluted with ethyl acetate (30 mL), washed with water (240 mL), brine (40 mL), and 30 dried (Na2SO4). After filtering, the extract was concentrated in vacuo and the desired product, as a mixture of E and Z-isomers, was isolated by column chromatography on silica gel, eluting with 5% ethyl acetate in petroleum ether. The purified oil solidified on standing at room temperature.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07449490B2 |
|---|
| 出典データセット | uspto-grants-2008_11 |
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| ORD ID | ord-f2ec646ed84c45559c6caa01c5677804 |
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| 出典メモ | uspto-grants-2008_11 |
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