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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227921Generated: October 24, 2026

3-Chlorobenzoic Acid → (1,1'-Biphenyl)-3-carboxylic acid

https://huagongshe.com/en/reaction/227921

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzoic AcidHCID 447—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
ReactantSodium 2'-(dicyclohexylphosphino)-2,6-dimethoxybiphenyl-3-sulfonateHCID 23677046—
Catalystpalladium(II) acetateHCID 167845—
Product(1,1'-Biphenyl)-3-carboxylic acidHCID 12854—

Reaction Steps

The general procedure described in Example 3 was used with 3-chlorobenzoic acid (157 mg, 1.00 mmol), phenylboronic acid (145 mg, 1.20 mmol), Pd(OAc)2 (4.5 mg, 0.020 mmol, 2 mol %), sodium 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl-3′-sulfonate (20.0 mg, 0.040 mmol, 4 mol %), K2CO3 (345 mg, 2.50 mmol), solvent (see FIG. 5) (2.0 mL), 14 h, temperature. The conversion and yield were determined using 1H NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560596B2
Source datasetuspto-grants-2009_07
ORD IDord-fa0ba15a14634939907da955358fc750
Source noteuspto-grants-2009_07