Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353286Erstellt: 24. Oktober 2026

Ethanol → (R)-3-(3-Fluorophenoxy)-3-phenylpropylamine

https://huagongshe.com/de/reaction/353286

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktAmmonium HydroxideHCID 14923—
EduktMaleic AcidHCID 444266—
Edukt(R)-3-(3-Fluorophenoxy)-3-phenylpropylchlorideHCID 39364375—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(R)-3-(3-Fluorophenoxy)-3-phenylpropylamineHCID 11593957—

Reaktionsschritte

A solution of (R)-3-(3-fluorophenoxy)-3-phenylpropyl chloride (0.971 g, 3.96 mmol), conc. NH4OH (30 mL) and EtOH (20 mL) were shaken at 90° C. on a Parr apparatus (50-90 psig) for 18 h. The mixture was then evaporated under vacuum and the residue was dissolved in Et2O (100 mL) and washed with H2O (2×25 mL). The organic layer was dried (anh. Na2SO4), filtered, and evaporated under vacuum to provide a yellow oil. This material was then dissolved in EtOAc (50 mL) and filtered. A solution of maleic acid (0.272 g, 2.6 mmol, 0.93 equiv) dissolved in hot EtOAc (5 mL) was added to precipitate the maleate salt (519 mg, 53.5%) as a white solid: TLC Rf 0.25 (1% MeOH—CHCl3); GC, tr 7.37 min; MS, m/z 245 (M+). The synthesis of Compound 187 was accomplished as follows.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06750244B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-c255f2bc87ad4cd28e1b018bb0f92a89
Quellennotizuspto-grants-2004_06