HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439547Generated: November 1, 2026
Sodium Carbonate → Ethyl 2-(3,4-dimethoxyphenyl)-4-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/439547
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3,4-Dimethoxyphenylboronic acid | HCID 2734702 | — |
| Reactant | Ethyl 2-bromo-4-(trifluoromethyl)benzoate | HCID 15766264 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Ethyl 2-(3,4-dimethoxyphenyl)-4-(trifluoromethyl)benzoate | HCID 15766263 | 94% |
Reaction Steps
263 g (0.885 mol) of ethyl 2-bromo-4-(trifluoromethyl)benzoate, 750 ml of 1,2-dimethoxyethane, 4 g of tetrakis(triphenylphosphine)palladium, 177 g (0.974 mol) of 3,4-dimethoxyphenylboronic acid and 1000 ml of a 2M aqueous sodium carbonate solution are introduced successively, under an inert atmosphere, into a four-liter round-bottomed flask. The reaction mixture is brought to reflux for fourteen hours and then evaporated to a third under reduced pressure. The reaction mixture is poured onto two liters of water; the precipitate which forms is filtered on sintered glass, rinsed with water and then dried under a stream of air. There is thus obtained 294 g (yield: 94%) of ethyl 2-(3,4-dimethoxyphenyl)-4-(trifluoromethyl)benzoate in the form of a beige solid melting at 89° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05514719 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-9e3d5b86151442e4a0337e966a23226f |
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| Source note | uspto-grants-1996_05 |
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