Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Methyl chloroformate | HCID 6586 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Carbamimidic acid, methyl ester, sulfate (1:1) | HCID 169039 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1,3-dimethoxycarbonyl-O-methylisourea | HCID 85348789 | — |
Reaktionsschritte
A three-neck flask fitted with a mechanical stirrer was charged with H2O (1.1 L), CH2Cl2 (1 L) and Na2CO3 (254.4 g, 2.4 mol) and the mixture chilled to ca 5° C. To the chilled mixture was then added the O-methylisourea hydrogen sulfate from above, tetrabutylammonium bromide (0.5 g) and methyl chloroformate (556 mL, 7.2 mol). The mixture was stirred vigorously and 25% NaOH (144 g in ca. 600 mL) was added over 0.5 h. After the last addition, the mixture was stirred for an additional 2 h and then filtered through Celite to remove inorganic salts (Na2SO4). The layers were separated and the organic layer dried (Na2SO4), filtered and concentrated to give the title compound as a thick syrup. The syrup was dried in vacuo overnight during which time it solidified to give 114.7 g (0.6 mol. 53%) of 1,3-dimethoxycarbonyl-O-methylisourea.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06946554B2 |
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| Quelldatensatz | uspto-grants-2005_09 |
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| ORD ID | ord-85697c4cfef349d48d942fc9e44a1f8b |
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| Quellennotiz | uspto-grants-2005_09 |
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