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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 62786Erstellt: 23. Oktober 2026

Methyl 4-chloro-3-(trifluoromethyl)benzoate → Methyl 4-cyclopentyl-3-(trifluoromethyl)benzoate

https://huagongshe.com/de/reaction/62786

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 4-chloro-3-(trifluoromethyl)benzoateHCID 14148738—
EduktHCID 178478989HCID 178478989—
KatalysatorZincchlorideHCID 3007855—
KatalysatorHCID 178418851HCID 178418851—
ProduktMethyl 4-cyclopentyl-3-(trifluoromethyl)benzoateHCID 1109766895,8%

Reaktionsschritte

To zinc(II) chloride (0.5 M solution in tetrahydrofuran, 88.0 mL, 44.0 mmol) was added cyclopentylmagnesium chloride (2 M solution in ether, 20.5 mL, 41.1 mmol). The resulting suspension was stirred at room temperature for 1 h. To the above suspension was added methyl 4-chloro-3-(trifluoromethyl)benzoate (7.00 g, 29.3 mmol) and bis(tri-tert-butylphosphine)palladium (1.35 g, 2.64 mmol) at room temperature. The mixture was heated under reflux for 2 h. The mixture was allowed to cool to room temperature, quenched with saturated aqueous sodium bicarbonate solution and filtered. The filtrate was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, concentrated under reduced pressure and purified by silica gel column chromatography to give the title compound as an oil (7.64 g). LCMS m/z=273.2 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 1.57-1.66 (m, 2H), 1.68-1.82 (m, 2H), 1.82-1.94 (m, 2H), 2.04-221 (m, 2H), 3.33-3.49 (m, 1H), 3.93 (s, 3H), 7.54 (d, J=8.21 Hz, 1H), 8.13 (dd, J=8.34, 1.77 Hz, H), 8.27 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447041B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-29512bd29e554b878e504848b3bc000a
Quellennotizuspto-grants-2016_09