HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530977Generated: October 30, 2026
Sodium Carbonate → Ethyl 2-cyclopropyl-6-ethoxy-4'-fluorobiphenyl-4-carboxylate
https://huagongshe.com/reaction/530977
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | Ethyl 2-ethoxy-4'-fluoro-6-(((trifluoromethyl)sulfonyl)oxy)biphenyl-4-carboxylate | HCID 117992433 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2-cyclopropyl-6-ethoxy-4'-fluorobiphenyl-4-carboxylate | HCID 90423848 | 89.4% |
Reaction Steps
A mixture of ethyl 2-ethoxy-4′-fluoro-6-(((trifluoromethyl)sulfonyl)oxy)biphenyl-4-carboxylate (15.6 g), cyclopropylboronic acid (7.67 g), dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine (2.20 g), a 2 M aqueous sodium carbonate solution (53.6 mL), tris(dibenzylideneacetone)dipalladium(0) (2.29 g), and toluene (60 mL) was stirred at 100° C. for 2 hours in an argon atmosphere. The reaction mixture was allowed to cool to room temperature and then poured to water, followed by extraction with ethyl acetate. The obtained organic layer was washed with saturated saline 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 (10.5 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-2a06ec2ca4b240edb06ada16407d1590 |
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| Source note | uspto-grants-2016_05 |
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