HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098926Generated: November 1, 2026
Dimethylformamide → Methyl 2-(1-cycloocten-1-yl)-2'-fluoro-5'-(methyloxy)-1,1'-biphenyl-4-carboxylate
https://huagongshe.com/reaction/2098926
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(1-Cycloocten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 46179848 | — |
| Reactant | Methyl 2'-fluoro-2-iodo-5'-(methyloxy)-1,1'-biphenyl-4-carboxylate | HCID 57705628 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Methyl 2-(1-cycloocten-1-yl)-2'-fluoro-5'-(methyloxy)-1,1'-biphenyl-4-carboxylate | HCID 67358853 | 49% |
Reaction Steps
To a stirred solution of T10.4 (0.750 g, 1.9 mmol) in DMF (4.00 mL, 52 mmol) at 23° C. was added (Z)-2-cyclooctenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane T11.3 (0.92 g, 3.9 mmol), potassium carbonate (0.81 g, 5.8 mmol), and then tetrakis(triphenylphosphine)palladium (0.22 g, 0.19 mmol). The mixture was heated at 90° C. for 19 hours and then cooled to room temperature. The reaction was 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 T11.4 as a colorless oil (0.35 g, 49% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450522B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-d64b1575874b4084af55c559f658b536 |
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| Source note | uspto-grants-2013_05 |
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