Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | D-Asparagine | HCID 439600 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | N-[4-methoxybenzenesulfonyl]-(D)-asparagine | HCID 27014145 | — |
Reaktionsschritte
D-asparagine (13.2 g, 100.0 mmol) is dissolved in dioxane 1,75.0 mL) and water (125.0 mL), triethylamine (21.0 mL, 150.0 mmol) is added, and the solution is cooled to 0° C. To this solution is added 4-methoxybenzenesulfonyl chloride (22.7 g, 110.0 mmol) over 10 minutes. The reaction is warmed to room temperature and stirred for 3 days. The precipitate is then filtered off, the filtrate is acidified to pH=~4, and extracted well with ethyl acetate. A first crop of pure product precipitates from the ethyl acetate and is collected by filtration. A second crop is obtained by evaporating off the ethyl acetate, and rinsing the solid obtained with water to remove inorganic salts. The two crops are combined to give N-[4-methoxybenzenesulfonyl]-(D)-asparagine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05455258 |
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| Quelldatensatz | uspto-grants-1995_10 |
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| ORD ID | ord-186a678734c54e59bc312368c8900fe1 |
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| Quellennotiz | uspto-grants-1995_10 |
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