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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055059Generated: October 30, 2026

Hydrochloric Acid → 4-Biphenylcarboxylic acid, 4'-chloro-

https://huagongshe.com/reaction/2055059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant4'-Chloro[1,1'-biphenyl]-4-carbaldehydeHCID 592570—
ReactantSodium BisulfiteHCID 23665763—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventChloroform methanolHCID 21584188—
SolventAcetone acetonitrileHCID 21918305—
Product4-Biphenylcarboxylic acid, 4'-chloro-HCID 616002—

Reaction Steps

To a stirred solution of 4-(4-chlorophenyl)benzaldehyde (0.84 g, 3.9 mmol) in 30 mL acetonitrile-acetone (2:1) is added 15 mL water and solid sodium bicarbonate (3.5 g, 41.7 mmol). After 5 min. a 25 mL solution of oxidation reagent (Oxone: 4.8 g, 7.8 mmol in 25 mL water containing 4×10−4 M EDTA) is added dropwise over 15 min. then stirred for an additional 3.5 h. The reaction mixture is then treated with 18 mL aq. sodium bisulfite (9.5 g), stirred 2 h, then acidified with 10 mL 6 M HCl. The mixture is transferred to a separatory funnel and diluted with 300 mL dichloromethane and 400 mL water. The water layer is washed with dichloromethane (3×120 mL), organic layers combined, then washed with 500 mL water. The organic layer is dried over sodium sulfate, filtered, and evaporated under reduced pressure. The desired acid is crystallized from acetone-water (5:2), filtered, washed with water, and evaporated under reduced pressure from toluene affording 0.6 g product. Remaining product could be isolated by chromatography but the amount obtained is satisfactory. TLC: Rf=0.3 (chloroform-methanol; 10:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07331920B2
Source datasetuspto-grants-2008_02
ORD IDord-97d240a28be14b8993979c6bd0e5d9ae
Source noteuspto-grants-2008_02