HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053688Generated: November 1, 2026
Methyl 4-bromobenzoate → HCID 69129920, compound
https://huagongshe.com/reaction/2053688
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-bromobenzoate | HCID 12081 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 3,4-Difluorobenzeneboronic acid | HCID 2734337 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69129920 | HCID 69129920 | — |
Reaction Steps
Combine 3,4-difluorobenzeneboronic acid (1.0 g, 5.2 mmol), methyl-4-bromobenzoate (0.241 g, 1.73 mmol), Pd(OAc)2 (0.019 g, 0.086 mmol), tetrabutylammonium bromide (0.111 g, 0.345 mmol), and potassium phosphate (0.733 g, 3.454 mmol). Purge the reaction vessel with argon and add anhydrous DMF (20 ml) to the reaction mixture. Heat the sealed reaction vessel to 120° C. with stirring until completion. Cool the reaction to room temperature, dilute with ethyl acetate, and filter through a short plug of celite with additional ethyl acetate. Wash organics with water, dry over MgSO4, filter, and evaporate. Purification by flash column chromatography yields 3′,4′-difluorobiphenyl-4-carboxylic acid methyl ester as a yellow solid. Dissolve the purified ester in dioxane (45 ml) and add an equal volume of 1 M aqueous NaOH. Heat the reaction vessel to 60° C. with stirring until completion. Remove the solvent by evaporation. Dissolve the residue in dichloromethane and wash with 1N aqueous hydrochloric acid. Dry the organics over MgSO4, filter and evaporate to yield 0.048 g (12%) of the title compound. MS (m/e): 235 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07326731B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-cf4b69aa35d44c7c9fca7c199860f9d1 |
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| Source note | uspto-grants-2008_02 |
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