HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21743Erstellt: 23. Oktober 2026
N-alpha-Benzyloxycarbonyl-L-lysine → N2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl Ester
https://huagongshe.com/de/reaction/21743
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N-alpha-Benzyloxycarbonyl-L-lysine | HCID 75172 | — |
| Lösungsmittel | tert-Butyl acetate | HCID 10908 | — |
| Lösungsmittel | Perchloric Acid | HCID 24247 | — |
| Produkt | N2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl Ester | HCID 11078219 | 72% |
Reaktionsschritte
Nα -(Benzyloxycarbonyl)-L-lysine (5.0 gm, 17.84 mmol) was dissolved in 268 ml of tert-butyl acetate containing 2.80 ml of perchloric acid (69-72% aqueous solution). The solution was stirred for 2 days at room temperature and then was extracted with water (3×200 ml). The combined aqueous layers were adjusted to pH 10 with 50% sodium hydroxide. The aqueous solution was then extracted with ethyl acetate (3×200 ml) and the organic layers dried over MgSO4. After filtration to remove MgSO4, the solvent was removed by evaporation at reduced pressure to provide Nα -(benzyloxycarbonyl)-L-lysine tert-butyl ester as a clear oil (2.16 gm, 36%). 1H NMR (CDCl3) 1.35 (s,9H), 1.40-2.0 (m,6H), 2.60 (t,2H), 4.10 (m, 1H), 4.98 (s,2H), 5.29 (bs,1H), 7.35 (s,5H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05424447 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-8224666d4e8f467c8cbd4d16ff05bd05 |
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| Quellennotiz | uspto-grants-1995_06 |
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