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HRID 62788作成日:2026年10月26日

Thionyl Chloride → 4-(Chloromethyl)-1-cyclopentyl-2-(trifluoromethyl)benzene

https://huagongshe.com/reaction/62788

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物(4-Cyclopentyl-3-(trifluoromethyl)phenyl)methanolHCID 58020942—
生成物4-(Chloromethyl)-1-cyclopentyl-2-(trifluoromethyl)benzeneHCID 5340260289.2%

反応条件

温度50 °C

反応手順

To (4-cyclopentyl-3-(trifluoromethyl)phenyl)methanol (1.21 g, 4.95 mmol) was added thionyl chloride (5.5 mL, 74.2 mmol). The mixture was heated at 50° C. for 2 h before it was allowed to cool to room temperature and stirred at room temperature overnight. The mixture was poured into ice and stirred for 5 min before it was extracted with dichloromethane. The organic extract was washed with saturated aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound as an oil (1.16 g). 1H NMR (400 MHz, CDCl3) δ ppm 1.55-1.63 (m, 2H), 1.69-1.77 (m, 2H), 1.82-1.90 (m, 2H), 2.05-2.13 (m, 2H), 3.37 (quintet, J=8.59 Hz, 1H), 4.58 (s, 2H), 7.46 (d, J=8.00 Hz, 1H), 7.52 (d, J=8.00 Hz, 1H), 7.61 (d, J=1.52 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447041B2
出典データセットuspto-grants-2016_09
ORD IDord-78e7b3514665431db39cfb3a8401b54a
出典メモuspto-grants-2016_09