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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915631Generated: November 1, 2026

Sodium Hydroxide → 3',4'-Difluoro[1,1'-biphenyl]-4-carboxylic acid

https://huagongshe.com/reaction/915631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 69129920HCID 69129920—
Solvent1,4-DioxaneHCID 31275—
Product3',4'-Difluoro[1,1'-biphenyl]-4-carboxylic acidHCID 2513427712%

Reaction Conditions

Temperature60 °C

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 dimethylformamide (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 magnesium sulfate, 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 1M aqueous sodium hydroxide. 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 magnesium sulfate, filter and evaporate to yield 0.048 g (12%) of the title compound. MS (m/e): 235 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265246B2
Source datasetuspto-grants-2007_09
ORD IDord-f9b75a9f02da46af89d91dcee72e7667
Source noteuspto-grants-2007_09