HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29061Erstellt: 24. Oktober 2026
Ethyl bromoacetate → (s)-[But-3-enyl-(1-phenyl-ethyl)-amino]-acetic acid ethyl ester
https://huagongshe.com/de/reaction/29061
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl bromoacetate | HCID 7748 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | But-3-enyl-((S)-1-phenyl-ethyl)-amine | HCID 10559173 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (s)-[But-3-enyl-(1-phenyl-ethyl)-amino]-acetic acid ethyl ester | HCID 10956339 | 94,5% |
Reaktionsschritte
To a solution of But-3-enyl-((S)-1-phenyl-ethyl)-amine (6.37 g, 36.4 mmol) in 150 mL of DMF at 0° C. is added K2CO3 (10.0 g, 72.8 mmol) in small portions. After stirring at 0° C. for 10 min, ethylbromoacetate (8.35 g, 54.6 mmol) izs added slowly. The reaction mixture, a white suspension, is stirred at r.t. overnight/16 hrs. The solution is diluted with 200 mL of ether, and washed with 3×100 ml of water. The crude product is purified by chromatography (hexane/CH2Cl2: 50/50) to give a pale liquid(8.5 g, 94.5%). (NMR and MS data confirmed, U-4117-58).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07419975B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-ba3faff163924c36bd90fcaa1113892f |
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| Quellennotiz | uspto-grants-2008_09 |
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