Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanolamine | HCID 700 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | N-Hydroxysuccinimide | HCID 80170 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | ethyl N-(2-hydroxyethyl)carbamate | HCID 223805 | — |
Reaktionsschritte
To a stirred solution of ethyl chloroformate (4 g, 0.037 mol.) and N-hydroxysuccinimide (6.3 g, 0.055 mol.) in 10 mL of DCM at 0° C. under nitrogen atmosphere was added N,N-Diisopropylethylamine (9.5 g, 0.055 mol) in 10 mL of DCM. The progress of the reaction was monitored by thin layer chromatography (TLC). After stirring for 3 hrs at room temperature, the reaction mixture was filtered and the precipitate was washed with 2×10 mL of dichloromethane. The combined filtrate was evaporated and dissolved in 20 mL of acetonitrile, cooled in an ice-bath and then added dropwise a solution of Ethanolamine 23 (3.3 mL, 2.5 eq). The resulting mixture was stirred at ice-bath temperature for 1 h and then overnight at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC). The reaction mixture was filtered, and the precipitate was washed with 2×10 mL DCM and dried over sodium sulfate. After removing the solvent under reduced pressure, the residue was purified by silica gel column chromatography to give ethyl (2-hydroxyethyl)carbamate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09096515B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-452b771435f541efa7498b17b2532eee |
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| Quellennotiz | uspto-grants-2015_08 |
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