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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19177Erstellt: 24. Oktober 2026

Ammonium Chloride → 2-(Benzhydrylidene-amino)-3-(1-fluoro-cyclopentyl)-propionic acid ethyl ester

https://huagongshe.com/de/reaction/19177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
EduktPotassium tert-butoxideHCID 23665647—
EduktTrifluoro-methanesulfonic acid 1-fluoro-cyclopentylmethyl esterHCID 86635233—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(Benzhydrylidene-amino)-3-(1-fluoro-cyclopentyl)-propionic acid ethyl esterHCID 8663523458%

Reaktionsschritte

To a solution of N-(diphenylmethylene)glycine ethyl ester (1.94 g, 7.26 mmol) in N,N-dimethylformamide (10 mL) at 0° C. was added solid potassium t-butoxide (0.89 g, 7.93 mmol) over 10 min and the resulting solution stirred for an additional 15 min. A trifluoro-methanesulfonic acid 1-fluoro-cyclopentylmethyl ester (2 g, 7.99 mmol) solution in N,N-dimethylformamide (2 mL) was added and the resulting mixture allowed to warm to room temperature over 2 h. The resulting mixture was poured into saturated ammonium chloride and extracted with dichloromethane (200 mL). The organic phase was separated, washed with saturated sodium chloride solution and dried over magnesium sulfate. The mixture was filtered and evaporated and the residue purified by AnaLogix flash chromatography (AnaLogix SuperFlash Flash Column 120 g, 10% to 20% ethyl acetate/hexanes) which afforded 2-(benzhydrylidene-amino)-3-(1-fluoro-cyclopentyl)-propionic acid ethyl ester (1.36 g, 58%) as a yellow oil: 1H NMR (300 MHz, CDCl3) δ ppm 1.26 (t, J=7.1 Hz, 3H), 1.39-1.97 (m, 8H), 2.11-2.41 (m, 1H), 2.45-2.76 (m, 1H), 4.01-4.27 (m, 2H), 4.37 (dd, J=7.5, 4.5 Hz, 1H), 7.16-7.25 (m, 2H), 7.29-7.41 (m, 3H), 7.41-7.56 (m, 3H), 7.64 (d, J=7.8 Hz, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741327B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-88643da42a2d4fc7b2df92278bd8a00b
Quellennotizuspto-grants-2010_06