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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353080Generated: October 30, 2026

Sodium Methoxide → HCID 17989405, compound

https://huagongshe.com/reaction/1353080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 17989336HCID 17989336—
ProductHCID 17989405HCID 17989405—

Reaction Conditions

Temperature100 °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-93184b7fe57345c3b93390b51c3accb2
Source noteuspto-grants-2007_05