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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257070Generated: October 26, 2026

Potassium Iodide → 2-(4'-Fluoro-4-biphenylylmethyl)-6-(2,2-dimethoxyethoxy)-1-oxo-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/257070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium hydrideHCID 24758—
Reactant4-(Bromomethyl)-4'-fluoro-1,1'-biphenylHCID 18963863—
Reactant6-(2,2-Dimethoxyethoxy)-1-oxo-1,2,3,4-tetrahydroisoquinolineHCID 18963883—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(4'-Fluoro-4-biphenylylmethyl)-6-(2,2-dimethoxyethoxy)-1-oxo-1,2,3,4-tetrahydroisoquinolineHCID 18963941—

Reaction Steps

To a solution of 6-(2,2-dimethoxyethoxy)-1-oxo-1,2,3,4-tetrahydroisoquinoline (5.79 g, 23.05 mmol) and 4'-fluoro-4-biphenylylmethyl bromide (9.16 g, 34.57 mmol), in DMF (100 ml) is added sodium hydride (1.1 g, 27.5 mmol) and a catalytic amount of potassium iodide. The reaction mixture is stirred for 2 hours at room temperature and is subsequently diluted with H2O (500 ml). The mixture is then extracted with EtOAc (2×300 ml). The combined EtOAc portions are washed with saturated NaCl solution (600 ml), dried over MgSO4, and concentrated in vacuo and washed with hexanes to yield the acetal, 2-(4'-fluoro-4-biphenylylmethyl)-6-(2,2-dimethoxyethoxy)-1-oxo-1,2,3,4-tetrahydroisoquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260316
Source datasetuspto-grants-1993_11
ORD IDord-7564cb1984e942478228cdf43ac8475e
Source noteuspto-grants-1993_11