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HRID 604779생성일: 2026년 10월 26일

Hydrochloric Acid → Isoquinolyl 4-methoxyphenyl ketone

https://huagongshe.com/reaction/604779

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-BromoanisoleHCID 7730—
반응물1,2-DibromoethaneHCID 7839—
반응물Sodium HydroxideHCID 14798—
반응물1-IsoquinolinecarbonitrileHCID 306057—
반응물MagnesiumHCID 5462224—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물Isoquinolyl 4-methoxyphenyl ketoneHCID 693112—

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온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910712B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-9a130f8005c04dfaa58a55f87d6fd8f3
출처 메모uspto-grants-2011_03