HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835460Generated: November 3, 2026
Sodium Carbonate → Methyl 5-(4-fluorophenyl)thiophene-2-carboxylate
https://huagongshe.com/reaction/1835460
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | Methyl 5-bromothiophene-2-carboxylate | HCID 605713 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Methyl 5-(4-fluorophenyl)thiophene-2-carboxylate | HCID 3263823 | 98.3% |
Reaction Steps
To a suspension of 2-bromo-5-methoxycarbonylthiophene (1.11 g), 4-fluorophenylboronic acid (0.91 g) and tetrakis(triphenylphosphine)palladium (289 mg) in 1,2-dimethoxyethane (10 ml) was added aqueous solution of sodium carbonate (2M, 6.5 ml) followed by stirring at 80° C. for 6 hours. The mixture was diluted with dichloromethane and washed with water and brine. The organic layer was dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by a silica gel column chromatography eluting with 30% dichloromethane in n-hexane to give 2-methoxycarbonyl-5-(4-fluorophenyl)thiophene (1.16 g, 98.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06770667B1 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-a3f5d724c0134cb68ca294b128eaead6 |
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| Source note | uspto-grants-2004_08 |
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