Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890731Generated: October 25, 2026

Water → 1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one

https://huagongshe.com/reaction/1890731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroacetoneHCID 6571—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 45074003—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-oneHCID 58318043—

Reaction Steps

A mixture containing 5-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride (1 g, 4 mmol), chloroacetone (407 mg, 4.4 mmol) and potassium carbonate (1.38 g, 10 mmol) in dimethyl formamide (DMF) (8 ml) is stirred at room temperature for 18 hours. To this mixture is added water (50 ml) and ethyl acetate (50 ml). The organic layer is separated, washed with brine, dried over MgSO4, and concentrated. The crude product is purified by flash column chromatography using 30% ethyl acetate in dichloromethane as eluent to give 1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one as an orange oil. LC-MS m/z: 269.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507491B2
Source datasetuspto-grants-2013_08
ORD IDord-af0443489ea74fdda2af49b22b005c94
Source noteuspto-grants-2013_08