HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 641584Erstellt: 25. Oktober 2026
3-(Trifluoromethyl)aniline → Benzyl 3-oxo-3-{[3-(trifluoromethyl)phenyl]amino}propanoate
https://huagongshe.com/reaction/641584
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | Diphenyl chlorophosphate | HCID 75654 | — |
| Edukt | Benzyl malonate | HCID 22247814 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Benzyl 3-oxo-3-{[3-(trifluoromethyl)phenyl]amino}propanoate | HCID 59666221 | — |
Reaktionsschritte
mono-Benzyl malonate (10 g) was dissolved in THF (100 ml), 4-methylmorpholine and cooled to −22° C. prior to the slow addition of diphenyl chlorophosphate (14 ml) and 3-trifluoromethyl-phenylamine (19 ml). After the reaction was warmed to rt overnight, it was heated to gently reflux for 0.5 h. After the reaction was cooled to rt, the solid was filtered off. The filtrate was concentrated. EtOAc was added along with 1N HCl solution. The organic layer was washed with NaHCO3 solution (aq) and brine, dried (MgSO4), filtered, and concentrated. Flash chromatography of the resulting residue gave N-(3-trifluoromethyl-phenyl)-malonamic acid benzyl ester (8.0 g): 1H NMR (CDCl3, δppm, 300 mHz) 3.56 (s, 2H), 5.26 (s, 2H), 7.40 (m, 7H), 7.75 (d, 1H), 7.83 (s, 1H), 9.43 (s, br, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07696205B2 |
|---|
| Quelldatensatz | uspto-grants-2010_04 |
|---|
| ORD ID | ord-05e0347d29644926bfb2ad1dffe84085 |
|---|
| Quellennotiz | uspto-grants-2010_04 |
|---|