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HRID 227552Erstellt: 24. Oktober 2026

3,5-Bis(trifluoromethyl)phenylacetic acid → (2R)-2-[4-{[3,5-bis(trifluoromethyl)phenyl]acetyl}-2-(3,4-dichlorophenyl)morpholin-2-yl]ethanol

https://huagongshe.com/de/reaction/227552

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-Bis(trifluoromethyl)phenylacetic acidHCID 123587—
Edukt(2R)-2-[2-(3,4-dichlorophenyl)morpholin-2-yl]ethanolHCID 10956756—
LösungsmittelAcetonitrileHCID 6342—
Produkt(2R)-2-[4-{[3,5-bis(trifluoromethyl)phenyl]acetyl}-2-(3,4-dichlorophenyl)morpholin-2-yl]ethanolHCID 8661294768,2%

Reaktionsschritte

To a solution of 3,5-bis(trifluoromethyl)phenylacetic acid (10.0 g, 36.8 mmol) in acetonitrile (100 ml), N,N′-carbonyldiimidazole (9.5 g, 58.8 mmol) was added at room temperature, then (2R)-2-[2-(3,4-dichlorophenyl)morpholin-2-yl]ethanol (17.3 g, 62.5 mol) was further added, and the resulting mixture was stirred at room temperature for 30 minutes. After completion of the reaction, the reaction mixture was evaporated to dryness. To the obtained residue, methylene chloride (100 ml), water (100 ml) and concentrated hydrochloric acid (15 ml) were added, and the resulting mixture was partitioned. The separated organic layer was washed with water twice (100 ml each) and evaporated to dryness. The residue obtained was purified by chromatography on a silica gel column to afford the title compound [13.3 g, yield: 68.1%] as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560549B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-802b123ba21541afbd5718208b30952e
Quellennotizuspto-grants-2009_07