HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dicyclohexylcarbodiimide → Fmoc-asn(trt)-opfp
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | Pentafluorophenol | HCID 13041 | — |
| Edukt | Fmoc-Asn(Trt)-OH | HCID 640248 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Fmoc-asn(trt)-opfp | HCID 15138257 | — |
Reaktionsschritte
1.5 g (2.51 mmol) of Fmoc-Asn(Trt)-OH are dissolved in 15 ml of tetrahydrofuran. 0.51 g (2.76 mmol) of pentafluoro-phenol is added, the solution is cooled to 0° and then 0.57 g (2.76 mmol) of dicyclohexyl-carbodiimide is also added in solid form. It is stirred at 0° for 30 minutes, at room temperature for 2 hours and again at 0° for 30 minutes. The dicyclohexylurea which has crystallized out is filtered off, and the filtrate is evaporated to dryness and triturated with 40 ml of diisopropyl ether. The powdery residue is filtered off, dried and recrystallized from methylene chloride/petroleum ether. Fmoc-Asn(Trt)-OPfp is obtained; m.p. 154°-156°, [α]D20 =-7.8° (THF).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05324833 |
| Quelldatensatz | uspto-grants-1994_06 |
| ORD ID | ord-81158b16d707489b8214ac7ac824e4a5 |
| Quellennotiz | uspto-grants-1994_06 |