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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505061Generated: October 23, 2026

3-Sulfolene → HCID 58317890, compound

https://huagongshe.com/en/reaction/1505061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-SulfoleneHCID 6498—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 45074003—
SolventWaterHCID 962—
SolventSodium BicarbonateHCID 516892—
ProductHCID 58317890HCID 58317890—

Reaction Conditions

Temperature70 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216964B2
Source datasetuspto-grants-2015_12
ORD IDord-cdd90c8f2b364f749a8d1cffc121e02d
Source noteuspto-grants-2015_12