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HRID 707756作成日:2026年10月26日

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

https://huagongshe.com/reaction/707756

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-chloro-3-(trifluoromethyl)benzoateHCID 14148738—
反応物HCID 178478989HCID 178478989—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418851HCID 178418851—
生成物Methyl 4-cyclopentyl-3-(trifluoromethyl)benzoateHCID 1109766895.8%

反応手順

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, 21H), 1.82-1.94 (m, 21H), 2.04-2.21 (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, 1H), 8.27 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09175320B2
出典データセットuspto-grants-2015_11
ORD IDord-d097ac3d570440c38a066a54181dc19c
出典メモuspto-grants-2015_11