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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15643Generated: October 26, 2026

Water → 3'-Fluoro-2',6'-dimethyl-4'-[3-(methylsulfonyl)propoxy]biphenyl-3-carbaldehyde

https://huagongshe.com/reaction/15643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-(Methylsulfonyl)propyl 4-methylbenzenesulfonateHCID 22732325—
Reactant3'-Fluoro-4'-hydroxy-2',6'-dimethylbiphenyl-3-carbaldehydeHCID 59342595—
SolventDimethylformamideHCID 6228—
Product3'-Fluoro-2',6'-dimethyl-4'-[3-(methylsulfonyl)propoxy]biphenyl-3-carbaldehydeHCID 5934257295%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 3′-fluoro-4′-hydroxy-2′,6′-dimethylbiphenyl-3-carbaldehyde (2.44 g, 10.0 mmol) and 3-(methylsulfonyl)propyl 4-methylbenzenesulfonate (3.51 g, 12.0 mmol) in N,N-dimethylformamide (20 mL) was added potassium carbonate (1.80 g, 13.0 mmol), and the mixture was stirred at 90° C. for 24 hr under nitrogen atmosphere. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed successively with 1 M aqueous sodium hydroxide solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=40:60-80:20), and the obtained crystals were recrystallized from heptane-ethyl acetate to give the title compound (3.45 g, yield 95%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732626B2
Source datasetuspto-grants-2010_06
ORD IDord-bcaf3887e9ce421bb3aa49e21271a9e2
Source noteuspto-grants-2010_06