HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 858576Erstellt: 25. Oktober 2026
Monoethyl malonate → (R)N-[1-(4-Bromo-phenyl)-ethyl]-malonamic Acid Ethyl Ester
https://huagongshe.com/reaction/858576
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Monoethyl malonate | HCID 70615 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | (R)-4-bromo-alpha-methylbenzylamine | HCID 853000 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (R)N-[1-(4-Bromo-phenyl)-ethyl]-malonamic Acid Ethyl Ester | HCID 58762223 | 71,1% |
Reaktionsschritte
To a magnetically stirred solution of (R)-(+)-1-(4-bromophenyl)ethylamine (0.51 g, 2.55 mmol) in anhydrous CH2Cl2 under argon and cooled to 0° C., were added ethyl hydrogen malonate (0.4 g, 3.06 mmol) EDC.HCl (0.58 g, 3.06 mmol) and HOBt (0.41 g, 3.06 mmol). The resulting solution was stirred at 25° C. overnight. CH2Cl2 was evaporate and residue partitioned between EtOAC and 1 N HCl. The organic layer was washed with H2O, brine and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by flash column chromatography (40% EtOAc in hexanes) to provide the desired product (0.57 g, 71%) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07148226B2 |
|---|
| Quelldatensatz | uspto-grants-2006_12 |
|---|
| ORD ID | ord-b69fd6196b72414d81b4d2877f6e7555 |
|---|
| Quellennotiz | uspto-grants-2006_12 |
|---|