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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1505061Erstellt: 25. Oktober 2026

3-Sulfolene → 5-Bromo-2-(1,1-dioxo-tetrahydro-thiophen-3-yl)-1,2,3,4-tetrahydro-isoquinoline

https://huagongshe.com/reaction/1505061

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-SulfoleneHCID 6498—
EduktPotassium HydroxideHCID 14797—
Edukt5-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 45074003—
LösungsmittelWaterHCID 962—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt5-Bromo-2-(1,1-dioxo-tetrahydro-thiophen-3-yl)-1,2,3,4-tetrahydro-isoquinolineHCID 58317890—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a solution containing 5-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride (1.5 g, 6 mmol) and butadiene sulfone (1.2 g, 10.2 mmol) in water (20 mL) is added 1N KOH (10 mL). The reaction mixture is stirred at 70° C. for 24 hours. After cooling to ambient temperature, the reaction mixture is diluted with saturated NaHCO3 solution and extracted with dichloromethane three times. The organic phase is washed with brine and dried over Na2SO4 before drying by rotary evaporation. The crude product is purified by silica gel flash chromatography to afford 5-bromo-2-(1,1-dioxo-tetrahydro-thiophen-3-yl)-1,2,3,4-tetrahydro-isoquinoline as a wax-like solid. MS m/z 330.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09216964B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-cdd90c8f2b364f749a8d1cffc121e02d
Quellennotizuspto-grants-2015_12