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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914990Generated: November 2, 2026

Benzene, 1-bromo-3-nitro- → 2-[3-(3-Nitrophenyl)prop-2-ynyl]-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/914990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-bromo-3-nitro-HCID 11457—
Reactant2-(Prop-2-yn-1-yl)-1,2,3,4-tetrahydroisoquinolineHCID 14341294—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventTriethylamineHCID 8471—
Product2-[3-(3-Nitrophenyl)prop-2-ynyl]-1,2,3,4-tetrahydroisoquinolineHCID 5895823266.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 81 (2.06 g, 10.2 mmol) in anhydrous triethylamine (30 mL) were sequentially added 1-bromo-3-nitrobenzene (1.83 g, 10.67 mmol), CuI (0.39 g, 2.05 mmol) and Pd(PPh3)4 (1.17 g, 1.0 mmol). The mixture was heated at 90° C. for 1 hour before it was filtered through Celite® and the filtrate was diluted with EtOAc (150 mL). The resulting solution was washed with water (100 mL), brine (100 mL), dried over Na2SO4 and concentrated. The residue was purified via flash silica gel chromatography to provide 93 (1.97 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265122B2
Source datasetuspto-grants-2007_09
ORD IDord-7263c587ce444de1ae78eb86f7fdb86f
Source noteuspto-grants-2007_09