HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27347Erstellt: 24. Oktober 2026
4-Methylmorpholine → carbobenzoxy-beta-alanyl-L-proline t-butyl ester
https://huagongshe.com/de/reaction/27347
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | Isobutyl chloroformate | HCID 62365 | — |
| Edukt | N-Benzyloxycarbonyl-beta-alanine | HCID 75313 | — |
| Edukt | tert-Butyl L-prolinate hydrochloride | HCID 6453107 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | carbobenzoxy-beta-alanyl-L-proline t-butyl ester | HCID 54135485 | — |
Reaktionsschritte
4.46 g. of carbobenzoxy-β-alanine is dissolved in 20 ml. of tetrahydrofuran and the resulting solution cooled to -10° C. With constant stirring of the solution, 2.4 ml. of N-methylmorpholine followed by 2.6 ml. of isobutylchloroformate are added and the resulting reaction mixture is stirred thereafter for approximately 5 minutes at -10° C. 4.16 g. of L-proline t-butyl ester hydrochloride in 20 ml. of dimethylformamide and 2.8 ml. of triethylamine is added to the reaction mixture which is thereafter stirred overnight, while slowly warming to room temperature. The solvent of the reaction mixture is evaporated in vacuo at 30°-35°. The residue is dissolved in 800 ml. of ethyl acetate which is washed with (2×150 ml.) a 10% citric acid solution, with (1×150 ml.) water, with (2×150 ml.) saturated solution of sodium bicarbonate and then with (2×100 ml.) water. The organic layer is dried with anhydrous magnesium sulfate and the solvent evaporated to yield carbobenzoxy-β-alanyl-L-proline t-butyl ester.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04221706 |
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| Quelldatensatz | uspto-grants-1980_09 |
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| ORD ID | ord-c7cd6af73aca49feafad7a587907044d |
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| Quellennotiz | uspto-grants-1980_09 |
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