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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431777Generated: November 1, 2026

1,4-Dibromobenzene → 2-(4-Bromophenyl)pyridine

https://huagongshe.com/reaction/431777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
Reactant2-BromopyridineHCID 7973—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Bromophenyl)pyridineHCID 151523771%

Reaction Steps

nBuLi (1.6M in hexanes, 34.4 mls, 55 mmol) was added dropwise to a stirred solution of 1,4-dibromobenzene (11.8 g, 50 mmol) in 100 ml of dry THF at −60° C. The mixture was stirred for 15 min at this temperature before a solution of ZnCl2 (0.5M in THF, 100 ml, 50 mmol) in THF was added dropwise. The mixture was allowed to warm to room temperature over 90 min, and then Pd(PPh3)4 (200 mg) was added, followed immediately by 2-bromopyridine (4.8 ml, 50 mmol). The whole was stirred at room temperature overnight, then evaporated to low (10 ml) volume and diluted with EtOAc (400 ml). The solution was washed with a solution of 32 g of EDTA in 200 ml water and brine (200 ml), dried (MgSO4) and evaporated to a yellow/green solid. This solid was purified by column chromatography using 1:1 hexane:DCM as eluant to provide the title product (8.3 g, 71%); m/z MH+234 (TS+); Found C 56.61%, H 3.37%, N 5.90%; Calcd. C 56.44%, H 3.44%, N 5.98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660756B2
Source datasetuspto-grants-2003_12
ORD IDord-ac438df0909c446e8c58fd6002e32ab1
Source noteuspto-grants-2003_12