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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238695Generated: October 26, 2026

3-Carboxyphenylboronic acid → 2'-Methoxy-3'-nitrobiphenyl-3-carboxylic acid

https://huagongshe.com/reaction/238695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Carboxyphenylboronic acidHCID 2733957—
Reactant1-Bromo-2-methoxy-3-nitrobenzeneHCID 22505713—
CatalystHCID 178418397HCID 178418397—
SolventSodium CarbonateHCID 10340—
Solvent1,4-DioxaneHCID 31275—
Product2'-Methoxy-3'-nitrobiphenyl-3-carboxylic acidHCID 9856767197.4%

Reaction Conditions

Temperature105 °C

Reaction Steps

1-Bromo-2-methoxy-3-nitro-benzene 1c (23.25 g, 0.10 mol), 3-carboxyphenylboronic acid (19.5 g, 117 mmol) and tetrakis(triphenylphosphine)palladium (8.86 g, 7.7 mol) were dissolved in a solvent mixture of 100 mL of 2 M sodium carbonate solution and 500 mL of 1,4-dioxane. The reaction mixture was heated to reflux at 105° C. for 43 hours. The mixture was concentrated under reduced pressure and then 300 mL of 6 N hydrochloric acid and 400 mL of ethyl acetate were added. The aqueous layer was extracted with ethyl acetate (200 mL×2). The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure to obtain the title compound 2′-methoxy-3′-nitro-biphenyl-3-carboxylic acid 1d (53.93 g) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642637B2
Source datasetuspto-grants-2014_02
ORD IDord-19e50ae11ac44868a31d61a5fc13bd02
Source noteuspto-grants-2014_02