HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → HCID 178498697, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methyl 2,3-dibromopropionate | HCID 95428 | — |
| Edukt | HCID 178498697 | HCID 178498697 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | HCID 178498697 | HCID 178498697 | 37% |
| Produkt | HCID 178498698 | HCID 178498698 | — |
Reaktionsschritte
To solution of methyl 2,3-dibromopropionate (25 mL, 198 mmol) in toluene at 5° C. was added triethylamine (55 mL, 0.39 mmol) in toluene (100 mL). After stirring for 5 min (S)-(1)-phenethylamine (25 mL, 198 mmol) in toluene (100 mL) was added dropwise. The suspension was refluxed for 3 h and allowed to cool down, filtered and the volatiles were evaporated under reduced pressure to give a residue that was purified by column chromatography (950 g of silica gel) with a gradient of 0-20% EtOAc in cyclohexane to yield to (S)-methyl 1-((S)-1-phenylethyl)aziridine-2-carboxylate EBE 06044A as a yellow oil (17.31 g, 43% yield) and (R)-methyl 1-((S)-1-phenylethyl)aziridine-2-carboxylate EBE 06044B as a yellow oil (15.14 g, 37% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08013000B2 |
| Quelldatensatz | uspto-grants-2011_09 |
| ORD ID | ord-a9b9d0c9110244e8a6a25754823db3d1 |
| Quellennotiz | uspto-grants-2011_09 |