Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Methyl 2,3-dibromopropionate | HCID 95428 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Katalysator | Trimethylamine oxide | HCID 1145 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Methyl 2-bromo-3-methoxypropanoate | HCID 352460 | — |
Reaktionsschritte
Methyl 2,3-dibromopropionate (21.9 g) and trimethylamine N-oxide (0.1 g) in methanol (8 ml) were cooled to −5° C. with stirring under an atmosphere of nitrogen. A methanolic solution of sodium methoxide, freshly prepared from sodium (2.25 g) and methanol (24 ml), was added dropwise over 15 minutes to the mixture, which was maintained below 0° C. by cooling. On complete addition, the mixture was stirred for a further 30 minutes then acetic acid (1 ml) was added followed by diethyl ether (100 ml). The mixture was filtered to remove insoluble salts and the filtrate evaporated under reduced pressure to give an oil, which was re-dissolved in a small volume of diethyl ether and re-filtered. The filtrate was evaporated under reduced pressure to give the required product (17.4 g) as a pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07122672B2 |
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| Quelldatensatz | uspto-grants-2006_10 |
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| ORD ID | ord-0ddadbb325e543c7a3e6936626446c66 |
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| Quellennotiz | uspto-grants-2006_10 |
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