HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phthalimide → tert-butyl-2(R)-[(tert-butoxycarbonyl)amino]-3-phthalimidopropionate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phthalimide | HCID 6809 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Edukt | (R)-3-(tert-Butoxy)-2-((tert-butoxycarbonyl)amino)propanoic acid | HCID 6992546 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | tert-butyl-2(R)-[(tert-butoxycarbonyl)amino]-3-phthalimidopropionate | HCID 18337585 | 62,6% |
Reaktionsschritte
To a solution of O-tert-butyl-N-BOC-D-serine (4 g, 15.31 mmol), phthalimide (3.38 g, 22.9 mmol) and triphenyl phosphine (6.03 g, 22.9 mmol) in tetrahydrofuran (120 ml, anhydrous) was added diisopropyl azodicarboxylate (4.5 ml, 22.9 mmol). The mixture was stirred under nitrogen atmosphere over night. The tetrahydrofuran was removed on the roto-evaporator and the remainder was taken up in methylene chloride (60 ml) and loaded onto a flash silica gel column. Elution with ethyl acetate/hexanes (19%) gave tert-butyl-2(R)-[(tert-butoxycarbonyl)amino]-3-phthalimido-propionate (3.74 g) as a white powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06844366B2 |
| Quelldatensatz | uspto-grants-2005_01 |
| ORD ID | ord-87b689c70e5c40dd84ed6c73d448be8d |
| Quellennotiz | uspto-grants-2005_01 |