HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662414Generated: October 30, 2026
Dimethylformamide → Dimethyl 2'-fluoro-1,1'-biphenyl-2,4-dicarboxylate
https://huagongshe.com/reaction/1662414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluorophenylboronic acid | HCID 2734354 | — |
| Reactant | 4-[[(Trifluoromethyl)sulfonyl]oxy]-1,3-benzenedicarboxylic acid dimethyl ester | HCID 12017546 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | Dimethyl 2'-fluoro-1,1'-biphenyl-2,4-dicarboxylate | HCID 57706591 | 82% |
Reaction Steps
To a stirred solution of dimethyl 4-(trifluoromethylsulfonyloxy)isophthalate 66.13B (1.60 g, 4.7 mmol) in DMF (9.4 mL, 4.7 mmol) at 23° C. was added 2-fluorophenylboronic acid (0.98 g, 7.0 mmol, commercially available from Aldrich), potassium carbonate (1.9 g, 14 mmol), and then tetrakis(triphenylphosphine)palladium (0.54 g, 0.47 mmol). The reaction mixture was heated to 90° C. and the reaction was stirred for 22 hours. The reaction was then cooled to room temperature, diluted with water, 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 then purified on silica gel (0-10% EtOAc in hexanes) to yield 66.32A as a colorless oil (1.10 g, 82% 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-fb5522aace9b4ea7a24a4bd533ab476b |
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| Source note | uspto-grants-2011_10 |
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