Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl butyrate | HCID 7762 | — |
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | Ethyl formate | HCID 8025 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 2-formylbutanoate | HCID 289299 | 194,4% |
| Produkt | Methyl acetate hexane | HCID 23449302 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09051331B2 |
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| Quelldatensatz | uspto-grants-2015_06 |
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| ORD ID | ord-2702fdc69c6d4d75ba4fa1eac5ea3e56 |
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| Quellennotiz | uspto-grants-2015_06 |
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