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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Trifluoromethyl)anilineHCID 7375—
Edukt4-MethylmorpholineHCID 7972—
EduktDiphenyl chlorophosphateHCID 75654—
EduktBenzyl malonateHCID 22247814—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzyl 3-oxo-3-{[3-(trifluoromethyl)phenyl]amino}propanoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07696205B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-05e0347d29644926bfb2ad1dffe84085
Quellennotizuspto-grants-2010_04