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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890732Generated: October 26, 2026

Cesium fluoride → 5-Bromo-2-(2,2-difluoropropyl)-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/1890732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(5-Bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-oneHCID 58318043—
CatalystTrifluoroacetic acidHCID 6422—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2-(2,2-difluoropropyl)-1,2,3,4-tetrahydroisoquinolineHCID 58317935—

Reaction Steps

To a solution of 1-(5-bromo-3,4-dihydroisoquinolin-2(1H)-yl)propan-2-one (962 mg, 3.59 mmol), diethylamino sulfur trifluoride (1.74 g, 10.8 ml) in DCM (12 ml) is added cesium fluoride (151 mg, 1 mmol) in small portions, then a few drops of TFA at room temperature. The mixture is stirred for 18 hours at room temperature. To this solution is added saturated aqueous NaHCO3 to quench the reaction. The aqueous layer is extracted with DCM (50 ml×3). The combined organic layers are washed with water, brine, dried over MgSO4 and concentrated. The residue is purified by silica gel flash chromatography, eluted with 20% ethyl acetate in hexanes to yield 5-Bromo-2-(2,2-difluoropropyl)-1,2,3,4-tetrahydroisoquinoline as a brown oil. LC-MS m/z: 291.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507491B2
Source datasetuspto-grants-2013_08
ORD IDord-8c5cf11f0e3f4776b1ac734ecd27e39d
Source noteuspto-grants-2013_08