HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662540Generated: October 30, 2026
Potassium Carbonate → HCID 57705786, compound
https://huagongshe.com/reaction/1662540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2,5-Difluorophenyl)boronic acid | HCID 2734335 | — |
| Reactant | Methyl 3-(5,5-dimethylcyclopent-1-enyl)-4-(trifluoromethylsulfonyloxy)benzoate | HCID 57467618 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 57705786 | HCID 57705786 | 93% |
Reaction Steps
To a stirred solution of methyl 3-(5,5-dimethylcyclopent-1-enyl)-4-(trifluoromethylsulfonyloxy)benzoate 66.6I (0.50 g, 1 mmol) in DMF (7 mL) at 23° C. was added 2,5-difluorophenylboronic acid (0.3 g, 2 mmol, commercially available from Aldrich), and potassium carbonate (0.5 g, 4 mmol). Tetrakis(triphenylphosphine)palladium (0.2 g, 0.1 mmol) was then added to the mixture. The mixture was heated to 90° C. and the reaction was further stirred for 23 hours. The reaction was then cooled to room temperature, diluted with brine and extracted three times with EtOAc. After drying over anhydrous magnesium sulfate and filtering, the organic solvent was removed under reduced pressure and the product was purified on silica gel (0-10% EtOAc in hexanes) to yield 83.25A as a colorless oil (0.42 g, 93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030354B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-2faad86d698d4f72b1fbdec2df3a4fa6 |
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| Source note | uspto-grants-2011_10 |
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