Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Beta-Alanine | HCID 239 | — |
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 2-carboxyethyldithiocarbamate | HCID 12458601 | — |
Reaktionsschritte
β-Alanine (17.8 g., 0.2 mol.) was added to a solution of 22.4 g. (0.4 mol.) of potassium hydroxide in 500 ml. of water at 25°. Carbon disulfide (12.2 ml., 0.2 mol.) was added and the reaction mixture was refluxed for three hours. The mixture was cooled, 28.4 g. (0.2 mol.) of methyl iodide and 500 ml. of ethanol were added and the resulting mixture was stirred for 30 minutes. The precipitate was collected by filtration, the filtrate was concentrated and the aqueous residue was combined with the solid material and brought to pH 8.5-9 by addition of 10% aqueous sodium hydroxide. The resulting suspension was extracted with ethyl acetate. Ethyl acetate was added to the aqueous phase which was then acidified to pH 1.5 with 6N hydrochloric acid. The layers were separated and the aqueous phase was extracted with ethyl acetate. The ethyl acetate extracts were combined, dried (MgSO4) and evaporated to dryness to give methyl 2-carboxyethyldithiocarbamate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04220644 |
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| Quelldatensatz | uspto-grants-1980_09 |
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| ORD ID | ord-1250061c6bf742d3bb1159de27181034 |
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| Quellennotiz | uspto-grants-1980_09 |
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