HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507973Generated: November 3, 2026
3-Formylphenylboronic acid → HCID 23157556, compound
https://huagongshe.com/reaction/507973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Formylphenylboronic acid | HCID 2734356 | — |
| Reactant | HCID 23157240 | HCID 23157240 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 23157556 | HCID 23157556 | 38.2% |
Reaction Steps
2-[(4-Bromo-3,5-dimethylphenyl)thio]ethyl ethyl ether (2.41 g, 8.33 mmol) and (3-formylphenyl)boronic acid (1.37 g, 9.16 mmol) were dissolved in a mixture of 2 M aqueous sodium carbonate solution (24 mL), ethanol (8 mL) and toluene (24 mL), the air was substituted with argon gas, and tetrakis(triphenylphosphine)palladium(0) (0.48 g, 0.42 mmol) was added. The reaction mixture was stirred under an argon atmosphere at 80° C. for 16 hr. After cooling the reaction mixture, saturated brine was added and the mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-hexane/ethyl acetate=5/1) to give the title compound (1.00 g, yield 38%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786165B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-95ba8aa4a29340d2bf67df53044e853d |
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| Source note | uspto-grants-2010_08 |
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