HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503108Generated: October 26, 2026
Hydrochloric Acid → (4'-Chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetic acid
https://huagongshe.com/reaction/1503108
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Reactant | 4-Chloro-3-fluorophenylboronic Acid | HCID 2778656 | — |
| Reactant | 2-(5-Bromo-2-methylphenyl)acetic acid | HCID 51063743 | — |
| Catalyst | Palladium acetylacetonate | HCID 5486778 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4'-Chloro-3'-fluoro-4-methylbiphenyl-3-yl)acetic acid | HCID 67375533 | — |
Reaction Steps
Under argon, 33.5 g (192 mmol) (4-chloro-3-fluorophenyl)boronic acid were added to a solution of 40.0 g (175 mmol) of (5-bromo-2-methylphenyl)acetic acid (EP 1791816 and WO 2006/29799) in a mixture of 437 ml (437 mmol) of degassed 1N aqueous sodium hydroxide solution, 160 ml of degassed water and 160 ml of degassed tetrahydrofuran. The mixture was stirred for 10 minutes, 507 mg (1.75 mmol) of tri-tert-butylphosphonium tetrafluoroborate and 532 mg (1.75 mmol) of palladium(II) acetylacetonate were added and the mixture was stirred at room temperature for 20 h. Toluene and water were then added, the pH was adjusted to 1-2 using concentrated aqueous hydrogen chloride solution, the mixture was stirred for 10 minutes, the phases were separated, the aqueous phase was extracted twice with toluene and the combined organic phases were dried over sodium sulphate, filtered and concentrated. The residue was stirred in 300 ml of a 6/1 mixture of n-hexane/tert-butyl methyl ether for 30 minutes, filtered off with suction, washed with n-hexane and dried under reduced pressure. This gave 38.0 g (78% of theory) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212140B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-d2c75b868e1e448d9b657370514d3115 |
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| Source note | uspto-grants-2015_12 |
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