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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990065Generated: October 31, 2026

Nitrogen → 2-(4-Bromophenyl)thiophene-3-carbonitrile

https://huagongshe.com/reaction/1990065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Bromophenyl)boronic acidHCID 79599—
Reactant2-Iodothiophene-3-carbonitrileHCID 10977399—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(4-Bromophenyl)thiophene-3-carbonitrileHCID 57975319—

Reaction Conditions

Temperature80 °C

Reaction Steps

Degass a solution of 2-iodo-thiophene-3-carbonitrile (20 g, 85 mmol), 4-bromobenzeneboronic acid (18.8 g, 94 mmol), potassium carbonate (26 g, 187 mmol) and tetrakis(triphenylphosphine)-palladium (0) (10 g, 8.5 mmol) in a mixture of anhydrous dimethoxyethane (300 mL) and absolute ethanol (150 mL) with Ar or N2 for 15 min and stir for 12 hours at 80° C. Cool the reaction mixture to room temperature, add water (100 ml) and extract the crude product dichloromethane (3×150 mL). Purification by chromatography (hexane-ethyl acetate 10/1) yields 16.3 g (72%) as a white solid: 1H NMR (CDCl3): δ 7.32 (m, 2H), 7.62 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642361B2
Source datasetuspto-grants-2010_01
ORD IDord-3836629298ae4afa8cc807ef58348857
Source noteuspto-grants-2010_01