Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Edukt | Methyl 3-(methylamino)but-2-enoate | HCID 2734182 | — |
| Produkt | Methyl acetyl(p-bromobenzoyl)acetate | HCID 603116 | — |
Reaktionsschritte
To 3-methylamino-but-2-enoic acid methyl ester (5.0 g, 39.1 mmol) in THF (70 mL) was added pyridine (3.7 mL). The mixture was cooled to 0° C., and 4-bromobenzoyl chloride (8.55 g, 39.1 mmol) in THF (30 mL) was added dropwise over 2 minutes. The reaction was warmed to room temperature over 1 hour and then stirred at room temperature overnight. Aqueous work-up gave the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08058300B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-29ad04ab882743a78678c693c4ae65f6 |
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| Quellennotiz | uspto-grants-2011_11 |
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