HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531071Generated: October 30, 2026
Sodium Carbonate → 6-Cyclopropyl-2,2',4'-trifluoro-3-methoxybiphenyl-4-carbaldehyde
https://huagongshe.com/reaction/531071
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | 6-Bromo-2,2',4'-trifluoro-3-methoxybiphenyl-4-carbaldehyde | HCID 117992108 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Cyclopropyl-2,2',4'-trifluoro-3-methoxybiphenyl-4-carbaldehyde | HCID 117992237 | 92% |
Reaction Steps
Cyclopropylboronic acid (1.01 g), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (0.323 g), a 2 M aqueous sodium carbonate solution (7.87 mL), and tris(dibenzylideneacetone)dipalladium(0) (0.360 g) were added at room temperature to a toluene (30 mL) solution of 6-bromo-2,2′,4′-trifluoro-3-methoxybiphenyl-4-carbaldehyde (1.36 g), and the mixture was stirred at 100° C. for 16 hours in an argon atmosphere. Water was added to the reaction mixture at room temperature, and the mixture was filtered through celite. Then, the filtrate was subjected to extraction with ethyl acetate. The obtained organic layer was washed with water and saturated saline in this order and dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (1.11 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353108B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-ea45e0aabcfc43539f69714332526f1f |
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| Source note | uspto-grants-2016_05 |
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