Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15653Generated: October 30, 2026

Water → 3'-Chloro-4'-hydroxy-2',6'-dimethylbiphenyl-3-carbaldehyde

https://huagongshe.com/reaction/15653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosuccinimideHCID 31398—
Reactant4'-Hydroxy-2',6'-dimethyl-[1,1'-biphenyl]-3-carbaldehydeHCID 23111691—
SolventDimethylformamideHCID 6228—
Product3'-Chloro-4'-hydroxy-2',6'-dimethylbiphenyl-3-carbaldehydeHCID 5934258265%

Reaction Steps

To a solution of 4′-hydroxy-2′,6′-dimethylbiphenyl-3-carbaldehyde (11.3 g, 50.0 mmol) in N,N-dimethylformamide (50 mL) was added N-chlorosuccinimide (6.68 g, 50.0 mmol) by small portions under ice-cooling, and the mixture was stirred at room temperature for 13 hr, and then at 50° C. for 3 hr. N-Chlorosuccinimide (1.34 g, 10.0 mmol) was added to the reaction mixture, and the mixture was stirred at the same temperature for 3 hr. N-Chlorosuccinimide (0.668 g, 5.00 mmol) was added again, and the mixture was further stirred at the same temperature for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-40:60), and the obtained crystals were recrystallized from ethyl acetate-heptane to give the title compound (8.47 g, yield 65%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732626B2
Source datasetuspto-grants-2010_06
ORD IDord-a4dcf1f8fcc040c4884b6640190b7d6b
Source noteuspto-grants-2010_06