HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460086Generated: October 29, 2026
4-Fluorophenylboronic acid → HCID 18444638, compound
https://huagongshe.com/reaction/460086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 18444641 | HCID 18444641 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18444638 | HCID 18444638 | 44.3% |
Reaction Steps
A mixture of (4-fluoro-phenyl)-boronic acid (300 mg, 2.1 mmoles), 3-(4-iodophenoxymethyl)-2-methyl-furan (123) (500 mg, 1.6 mmoles) and potassium acetate (0.6 g) in N,N-dimethylformamide (70 mL) was degassed, treated with [1,1′-bis(diphenylphosphino) ferrocene]dichloropalladium(II) complex with dichloromethane (1:1) (90 mg) and the mixture was agitated at 95° C. for 12 hours under an argon atmosphere. The mixture was concentrated in vacuo, partitioned between water (100 ml) and diethyl ether (200 ml). The aqueous phase was re-extracted with diethyl ether, and the combined etheral phases were dried and evaporated. The residue was purified by flash chromatography, using diethyl ether as eluent, to afford compound 124(200 mg) as a solid. This material was used directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196089B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-098435adcb8f4df793aa38a91638a42e |
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| Source note | uspto-grants-2007_03 |
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