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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353081Generated: October 30, 2026

Sodium Perborate → HCID 17989360, compound

https://huagongshe.com/reaction/1353081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium PerborateHCID 517072—
ReactantHCID 17989405HCID 17989405—
SolventAcetic AcidHCID 176—
ProductHCID 17989360HCID 1798936041%

Reaction Conditions

Temperature50 °C

Reaction Steps

4′-Chloro-3-(1,1-dichloromethyl)-4-nitrobiphenyl (0.4 g, 1.26 mmol) was dissolved in methanolic sodium methoxide (15 mL; 0.5 M). The mixture was refluxed for 12 hours under argon. The solvent was evaporated and the residue diluted in 1,4-dioxane (15 ml) and water (1 ml), then a few drops of concentrated HCl were added. The reaction mixture was stirred at 100° C. for 4 hours. The solvent was then evaporated and the crude mixture purified by flash chromatography on silica gel (eluting with dichloromethane in petroleum ether) to yield the 4′-chloro-4-nitrobiphenyl-3-carbaldehyde (0.32 g, 1.26 mmol); m/z (APCI−) 260 (40%, [M−H]−), 231 (100%). This aldehyde (0.32 g, 1.26 mmol) was dissolved in acetic acid (5 mL) and sodium perborate (0.23 g, 1.5 mmol) was added. The resulting mixture was stirred at 50° C. for 16 h. The mixture was cooled, the solvent was evaporated, ethyl acetate was added and the organic layer washed with water, dried over MgSO4 and evaporated to yield the 4′-chloro-4-nitrobiphenyl-3-carboxylic acid (0.14 g, 41%); m/z [APCI−] 276 (100%, [M−H−], 247 (60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220777B2
Source datasetuspto-grants-2007_05
ORD IDord-0cbcb21f81f748c08a2c301b3077c3ff
Source noteuspto-grants-2007_05