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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | (4-Chloro-2-methylphenyl)boronic acid | HCID 5017600 | — |
| Reactant | 4,5-Dibromothiophene-2-carbonitrile | HCID 23262276 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,5-Bis(4-chloro-2-methylphenyl)thiophene-2-carbonitrile | HCID 68293634 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012655B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-8bdaa99b9d2843429bd42ddfd2ead309 |
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| Source note | uspto-grants-2015_04 |
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