Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1900542Erstellt: 24. Oktober 2026

Dichloromethane → 3,4-Dihydroisoquinoline

https://huagongshe.com/reaction/1900542

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
Edukt1,2,3,4-TetrahydroisoquinolineHCID 7046—
EduktSodium HydroxideHCID 14798—
EduktPotassium PersulfateHCID 24412—
KatalysatorNickel sulfate hexahydrateHCID 5284429—
LösungsmittelWaterHCID 962—
Produkt3,4-DihydroisoquinolineHCID 76705—

Reaktionsschritte

Into a 5000 ml, 3-neck round-bottom flask equipped with a mechanical stirrer is placed 1,2,3,4-tetrahydroisoquinoline (1) (25.005 g) and methylene chloride (750 ml). A solution of potassium persulfate (71.376 g) and sodium hydroxide (18.0456 g) in deionized water (1650 ml) is added. While vigorously stirring the biphasic mixture, a solution of nickel sulfate hexahydrate (0.6499 g) in deionized water (75 ml) is added dropwise to the mixture. The reaction is allowed to stir overnight at room temperature. The biphasic mixture is vacuum filtered through Celite, the phases separated and the water layer extracted (3×300 ml) with methylene chloride. The organics are combined, dried with MgSO4 and reduced by rotary evaporation to a thick, dark brown oil. The desired product is isolated from the oil by Kugelrohr distillation (0.1 mm Hg, 75° C.). The preparation is represented by the following reaction: ##STR26##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05576282
Quelldatensatzuspto-grants-1996_11
ORD IDord-1ef48c0ba78547a19b220b759a7f2b3e
Quellennotizuspto-grants-1996_11