HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 256490Erstellt: 25. Oktober 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → BOC-Ala-Gly-OBzl
https://huagongshe.com/reaction/256490
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Edukt | O-benzylglycine toluene-p-sulphonate | HCID 6451311 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | BOC-Ala-Gly-OBzl | HCID 10980600 | 92,4% |
Reaktionsschritte
To a solution of 5.68 g of BOC-Ala-OH, 10.12 g of H-Gly-OBzl.TosOH and 4.0 g of HOBT dissolved in 50 ml of THF, under cooling at -5° C., was added 5.5 ml of WSC, and the mixture was stirred at -5° C. for one hour and at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate. The ethyl acetate layer was washed successively twice with 1N hydrochloric acid, twice with 5% aqueous sodium hydrogen carbonate and with water. After drying over anhydrous magnesium sulfate, the product was concentrated under reduced pressure. The residue was crystallized from n-hexane, then recrystallized twice from ethyl acetate-n-hexane to give 9.32 g (yield: 92.3%) of BOC-Ala-Gly-OBzl melting at 85°-87° C. Rf1 =0.54.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04703106 |
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| Quelldatensatz | uspto-grants-1987_10 |
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| ORD ID | ord-13ab10030a7b4817b32c19cc963e4370 |
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| Quellennotiz | uspto-grants-1987_10 |
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