HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47045Erstellt: 25. Oktober 2026
Benzoyl chloride → N-benzoyl-L-alanyl-L-proline ethylamide
https://huagongshe.com/reaction/47045
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzoyl chloride | HCID 7412 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | L-alanyl-L-proline ethylamide hydrobromide | HCID 70602162 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-benzoyl-L-alanyl-L-proline ethylamide | HCID 54309979 | 68,9% |
Reaktionsschritte
1.42 g (0.0048 mol) of L-alanyl-L-proline ethylamide hydrobromide were dissolved in 20 ml of methylene chloride, 21.8 ml (0.01 mol) of 0.5-N sodium hydroxide solution were added followed by 0.54 ml (0.0053 mol) of benzoyl chloride. The mixture was stirred vigorously at room temperature for 1 hour with care being taken that the solution remained basic, this being achieved by the addition of a few drops of 0.5-N sodium hydroxide solution. The layers were then allowed to separate and the methylene chloride layer was separated, dried over magnesium sulphate and evaporated to an oil which crystallised on treatment with ethyl acetate. The crystals were filtered off, washed and dried to yield 1.05 g of N-benzoyl-L-alanyl-L-proline ethylamide of melting point 200°-202° C.; [α]D20 =-82.7° (c=0.99 in methanol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04176116 |
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| Quelldatensatz | uspto-grants-1979_11 |
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| ORD ID | ord-00cb2a1f19a44f2d8f439eb07dc5a70f |
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| Quellennotiz | uspto-grants-1979_11 |
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