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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472769Generated: October 30, 2026

Sodium Carbonate → 4,5-Bis(4-chloro-2-methylphenyl)thiophene-2-carbonitrile

https://huagongshe.com/reaction/1472769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,4-DioxaneHCID 31275—
Reactant(4-Chloro-2-methylphenyl)boronic acidHCID 5017600—
Reactant4,5-Dibromothiophene-2-carbonitrileHCID 23262276—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product4,5-Bis(4-chloro-2-methylphenyl)thiophene-2-carbonitrileHCID 6829363484%

Reaction Conditions

Temperature90 °C

Reaction Steps

A round-bottomed flask was charged with 4,5-dibromothiophene-2-carbonitrile (534 mg, 2.00 mmol), 4-chloro-2-methylphenylboronic acid (818 mg, 4.80 mmol) and Pd(PPh3)4 (136 mg, 0.10 mmol). After degassed, dioxane (10 mL) and aqueous sodium carbonate (5 mL, 2M, 10 mmol) was added. The reaction mixture was heated to 90° C. The progress of the reaction was monitored by TLC. After the reaction was complete, 50 mL of water was added, and the reaction mixture was extracted with ethyl acetate. The organic phase was dried over anhydrous sodium sulphate and then concentrated. The residue was purified by flash chromatography (hexane:CH2Cl2=2:1). 0.60 g (84%) of product was obtained as clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012655B2
Source datasetuspto-grants-2015_04
ORD IDord-8bdaa99b9d2843429bd42ddfd2ead309
Source noteuspto-grants-2015_04