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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1982765Erstellt: 25. Oktober 2026

Hydrochloric Acid → Isoquinolyl 4-methoxyphenyl ketone

https://huagongshe.com/reaction/1982765

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-BromoanisoleHCID 7730—
Edukt1,2-DibromoethaneHCID 7839—
EduktSodium HydroxideHCID 14798—
Edukt1-IsoquinolinecarbonitrileHCID 306057—
EduktMagnesiumHCID 5462224—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktIsoquinolyl 4-methoxyphenyl ketoneHCID 693112—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07541332B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-1a85056b9fc048c58f95a262c570ccc7
Quellennotizuspto-grants-2009_06