Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36127Erstellt: 24. Oktober 2026

Ethanol → N-Boc-4-cyanophenylalanine-N-methylamide

https://huagongshe.com/de/reaction/36127

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktMethylamineHCID 6329—
Edukt4-MethylmorpholineHCID 7972—
EduktPentafluorophenolHCID 13041—
EduktN-(tert-Butoxycarbonyl)-4-cyano-L-phenylalanineHCID 7020841—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-Boc-4-cyanophenylalanine-N-methylamideHCID 2285121092%

Reaktionsschritte

A solution of N-Boc-4-cyanophenylalanine (1.92 g, 6.6 mmol) and pentafluorophenol (2.43 g, 13.2 mmol) in CH2Cl2 (30 ml) at 0° C. was treated with 4-methylmorpholine (0.74 g, 7.3 mmol). After stirring the reaction mixture for 3 hours, 8M methylamine in ethanol (15 ml, 19.8 mmol) was added and the reaction mixture left to stir at room temperature for 16 hours. The solvent was removed under pressure, the residue dissolved in CH2Cl2 (50 ml) and washed with saturated sodium bicarbonate (2×50 ml), 1M citric acid (2×50 ml) and brine (50 ml). The CH2Cl2 layer was dried over MgSO4 and the solvent removed under pressure to yield the title compound as a white solid (1.84 g, 92%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05412145
Quelldatensatzuspto-grants-1995_05
ORD IDord-a67bf3e8d4a2491c9a876d6e5cb62b11
Quellennotizuspto-grants-1995_05