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HRID 2108876作成日:2026年10月26日

Chloroform → 4-[(5-Bromopentyl)sulfanyl]-7-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/2108876

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物1,5-DibromopentaneHCID 8100—
反応物Potassium CarbonateHCID 11430—
反応物HCID 178506078HCID 178506078—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
生成物4-[(5-Bromopentyl)sulfanyl]-7-(trifluoromethyl)quinolineHCID 1797581572%

反応条件

温度20 °C

反応手順

7-Trifluoromethyl-4-quinoline-thiol (5 g, 21.8 mmol), 1,5-dibromopentane (23.7 g, 98.1 mmol) and CHCl3 (60 mL) were charged in a 250 ml round-bottomed flask equipped with a magnetic stirrer. TBABr (0.7 g, 2.2 mmol) and water (40 mL) were added and the reaction mixture was stirred for 48 h at 20° C. The reaction mixture was poured in 100 mL of H2O with K2CO3 (3.0 g, 21.8 mmol) and extracted with CH2Cl2 (400 mL). The organic layer was washed with water (30 mL), brine (2×30 mL), dried over MgSO4, filtered and evaporated at 30° C. to dryness. The crude compound was purified by column chromatography (SiO2:CH2Cl2:MeOH=99.5:0.5 to 98:2) to give after evaporation 4-(5-bromopentylthio)-7-(trifluoromethyl)quinoline 25 (5.9 g, 72% yield) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07514432B2
出典データセットuspto-grants-2009_04
ORD IDord-5ddb69884b0e43a7837a8afe289ae646
出典メモuspto-grants-2009_04