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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409362Generated: October 28, 2026

1-Bromo-2-chloro-4-iodobenzene → 2-(4-Bromo-3-chlorophenyl)thiophene

https://huagongshe.com/reaction/409362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-chloro-4-iodobenzeneHCID 2756886—
Reactant2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
ReactantEthyl acetate hexaneHCID 21226206—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product2-(4-Bromo-3-chlorophenyl)thiopheneHCID 57994054—

Reaction Steps

To a mixture of 1-bromo-2-chloro-4-iodobenzene (2.0 g, 6.30 mmol) in dioxane 30 mL, 2-tributylstannyl thiophene (2.352 g, 6.30 mmol), and 5% equivalent of Pd(PPh3)4 (0.364 g, 0.3155 mmol) is refluxed under nitrogen for 5 h. After cooling and evaporation of the solvent, the residue is dissolved in EtOAc 50 mL. 10% KF 30 mL is added and the solution is stirred at r.t. for 30 min. The resultant precipitate is removed by filtration. The solution is washed with water 20 mL×3, and dried with Na2SO4 and concentrated. The pure product (1.2 g, 4.39 mmol, white solid) is obtained by column chromatography using EtOAc/Hexane, 1-3% ration solvent system. 1H-NMR (CDCl3/300 MHz): 7.74 (d, J=2.1 Hz, 1H), 7.65 (d, J=7.2 Hz, 1H), 7.37 (m, 3H), 7.14 (m, 1H). MS (ES−, m/z): 529.2 (M+−Br, 20.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759384B2
Source datasetuspto-grants-2014_06
ORD IDord-01825ac4a1b8463888a3bdc7b1eec4e0
Source noteuspto-grants-2014_06