関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl butyrate | HCID 7762 | — |
| 反応物 | Diisopropylamine | HCID 7912 | — |
| 反応物 | Ethyl formate | HCID 8025 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Ethyl 2-formylbutanoate | HCID 289299 | 194.4% |
| 生成物 | Methyl acetate hexane | HCID 23449302 | — |
反応手順
A solution of diisopropylamine (10.1 g, 100 mmol) in THF (100 mL) was treated with n-butyllithium (1.6 M in hexane, 63 mL, 100 mmol) at room temperature under N2. The resulting pale yellow solution was cooled to −78° C. A solution of butyric acid ethyl ester (10.4 g, 89.2 mmol) in THF (28 mL) was added. Stirring was continued for a half hour at −78° C., after which ethyl formate (22.0 g, 300 mmol) was added. The reaction mixture was allowed to warm to room temperature and stirred for three hours under N2. The reaction mixture was quenched with acetic acid (˜17 ml), diluted with diethyl ether, washed with water, brine, dried (Na2SO4). Silica gel chromatography (methyl acetate/hexane) provided 12.5 g of the title compound as a mixture of isomers.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09051331B2 |
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| 出典データセット | uspto-grants-2015_06 |
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| ORD ID | ord-2702fdc69c6d4d75ba4fa1eac5ea3e56 |
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| 出典メモ | uspto-grants-2015_06 |
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