HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2,4,6-Trifluorobenzyl bromide → Methylamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2,4,6-Trifluorobenzyl bromide | HCID 2777059 | — |
| Edukt | Methyl 1-(4-hydroxyphenyl)-5-oxopyrrolidine-3-carboxylate | HCID 2883518 | — |
| Edukt | (RS)-5-oxo-1-[4-(3,4,5-trifluoro-benzyloxy)-phenyl]-pyrrolidine-3-carboxylic acid methyl ester | HCID 68615462 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Methylamine | HCID 6329 | — |
| Produkt | (RS)-5-oxo-1-[4-(3,4,5-trifluoro-benzyloxy)-phenyl]-pyrrolidine-3-carboxylic acid methylamide | HCID 10384975 | — |
Reaktionsschritte
The title compound is prepared by alkylation of the (RS)-1-(4-hydroxyphenyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl ester with 2,4,6-trifluorobenzyl bromide giving the (RS)-5-oxo-1-[4-(3,4,5-trifluoro-benzyloxy)-phenyl]-pyrrolidine-3-carboxylic acid methyl ester as a white solid (99% of theory) which, thereupon, by treatment with methylamine in ethanol at 50° C. yields the (RS)-5-oxo-1-[4-(3,4,5-trifluoro-benzyloxy)-phenyl]-pyrrolidine-3-carboxylic acid methylamide. Yield: 99% of theory as a white solid; MS: m/e=379 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07122562B2 |
| Quelldatensatz | uspto-grants-2006_10 |
| ORD ID | ord-9e4fe24ebd284e9990a7cbff83af1d54 |
| Quellennotiz | uspto-grants-2006_10 |