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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62783Erstellt: 25. Oktober 2026

Cyclopentanone → 1-(2-(Trifluoromethyl)phenyl)cyclopentanol

https://huagongshe.com/reaction/62783

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopentanoneHCID 8452—
EduktBenzene, 1-bromo-2-(trifluoromethyl)-HCID 9806—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(2-(Trifluoromethyl)phenyl)cyclopentanolHCID 6280214048,9%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of 1-bromo-2-(trifluoromethyl)benzene (0.5 g, 2.222 mmol) in anhydrous THF (10 mL) was cooled to −78° C. (dry ice IPA bath) under argon atmosphere. BuLi (2.5 M in hexanes, 1.068 mL, 2.67 mmol) was added in drops with efficient stirring. The reaction mixture was stirred at −78° C. for 40 min. A solution of cyclopentanone (0.243 g, 2.89 mmol) in anhydrous THF (1.5 mL) was added slowly (in drops) at −78° C. The reaction mixture was stirred at −78° C. for 30 min, gradually brought to room temperature, and stirred for 1 h. The reaction mixture was cooled by an ice bath, quenched with water, and acidified to pH 4-5 by addition of concentrated HCl. The solvent was removed under reduced pressure. The residue was dissolved in methylene chloride, washed with water (2 times), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography to give the title compound as an oil (250 mg). LCMS m/z=213.1 [M−H2O+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447041B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-47fe68485ad74b8da690b0ca7fd0be1b
Quellennotizuspto-grants-2016_09