HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261498Generated: November 3, 2026
2-Bromothiophene → 2-(2-Methoxyphenyl)thiophene
https://huagongshe.com/reaction/2261498
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Methoxyphenylboronic acid | HCID 2733958 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-(2-Methoxyphenyl)thiophene | HCID 3564190 | 95% |
Reaction Steps
2-Bromothiophene (7.2 g, 43.9 mmol), 2-methoxyphenylboronic acid (6.7 g, 43.9 mmol), palladium acetate (0.14 g, 0.62 mmol), triphenylphosphine (0.6 mg, 2.3 mmol) and potassium phosphate (9.40 g, 44.3 mmol) were added to a flask. A mixture solution of 10 mL of water and 40 mL of dimethoxyethane was added and reflux was performed for 6 hours. After cooling to room temperature, aqueous ammonium chloride solution (50 mL) and diethyl ether (100 mL) were added. The organic layer was separated. After extracting the residue using diethyl ether, the collected organic layer was dried with magnesium sulfate. After removing volatile materials, followed by purification via silica gel chromatography using hexane, 7.9 g (yield: 95%) of 2-(2′-methoxyphenyl)thiophene was obtained as colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07847039B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-d7d2d4a2c62e43c1871b8c18f0c2da81 |
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| Source note | uspto-grants-2010_12 |
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