HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465960Generated: November 3, 2026
4-Fluorophenylboronic acid → HCID 67232695, compound
https://huagongshe.com/reaction/1465960
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 67234158 | HCID 67234158 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67232695 | HCID 67232695 | 50.6% |
Reaction Steps
3-Bromo-2-(4-fluoro-phenyl)-7-hydroxy-thieno[3,2-c]pyridine-6-carboxylic acid methyl ester (0.34 g, 0.89 mmol), example 36-g, 4-fluoro-phenyl boronic acid (0.373 mg, 2.67 mmol), sodium methoxide (0.433 g, 8.01 mmol), and tetrakis(triphenylphosphine)palladium(0) (257 mg, 0.22 mmol) were suspended in 15 mL of 1,4-dioxane. The reaction mixture was heated at 120° C. for 30 min. using a CEM microwave reactor (CEM, Matthews, N.C.). The reaction mixture was diluted with ethyl acetate, and washed with saturated sodium bicarbonate and brine solutions. The organic fraction was dried over anhydrous sodium sulfate and concentrated. The crude product was purified by flash chromatography eluting from silica gel with a gradient of 0-60% ethyl acetate in hexanes to produce 0.179 g of a yellow solid. MS: (+) m/z 398.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000006B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-199d132a33d54d72b0ccb3fe79f9068e |
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| Source note | uspto-grants-2015_04 |
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