戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1673081作成日:2026年10月25日

Hydrochloric Acid → Isoquinolyl 4-methoxyphenyl ketone

https://huagongshe.com/reaction/1673081

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-BromoanisoleHCID 7730—
反応物1,2-DibromoethaneHCID 7839—
反応物Sodium HydroxideHCID 14798—
反応物1-IsoquinolinecarbonitrileHCID 306057—
反応物MagnesiumHCID 5462224—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物Isoquinolyl 4-methoxyphenyl ketoneHCID 693112—

反応条件

温度0 °C

反応手順

4-Bromoanisol (15.3 ml, 122 mmol) and a catalytic amount of 1,2-dibromoethane as an initiator were added to a mixed solution of magnesium (3059 mg, 125.8 mmol) and tetrahydrofuran (20 ml) under nitrogen atmosphere, and this reaction mixture was stirred while heating under reflux for 45 minutes. The mixture was cooled to 0° C., a solution of 1-isoquinolinecarbonitrile (10.78 g, 69.9 mmol) in tetrahydrofuran (30 ml) was added dropwise thereto, and this reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was cooled on ice, concentrated hydrochloric acid (24 ml) and methanol (120 ml) were added, and this mixture was heated under reflux for 1.5 hours. After cooling on ice, the mixture was adjusted to pH 8 by adding aqueous sodium hydroxide, extracted with ether, washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (15.87 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07999090B2
出典データセットuspto-grants-2011_08
ORD IDord-96c4f83336bc448c9400fff713a309f0
出典メモuspto-grants-2011_08