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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453441Generated: October 26, 2026

Water → (3'-(Hydroxymethyl)-6-methyl-4-[3-(methylsulfonyl)propoxy]biphenyl-2-yl)methyl acetate

https://huagongshe.com/reaction/453441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-(Methylsulfonyl)propyl 4-methylbenzenesulfonateHCID 22732325—
Reactant[4-Hydroxy-3'-(hydroxymethyl)-6-methylbiphenyl-2-yl]methyl acetateHCID 59342611—
SolventDimethylformamideHCID 6228—
Product(3'-(Hydroxymethyl)-6-methyl-4-[3-(methylsulfonyl)propoxy]biphenyl-2-yl)methyl acetateHCID 5934257360.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of [4-hydroxy-3′-(hydroxymethyl)-6-methylbiphenyl-2-yl]methyl acetate (1.02 g, 3.56 mmol) and 3-(methylsulfonyl)propyl 4-methylbenzenesulfonate (1.25 g, 4.27 mmol) in N,N-dimethylformamide (10 mL) was added potassium carbonate (0.640 g, 4.32 mmol), and the mixture was stirred at 90° C. for 21 hr under nitrogen atmosphere. 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=50:50-100:0) to give the title compound (0.87 g, yield 60%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492430B2
Source datasetuspto-grants-2013_07
ORD IDord-f95f4c9b1f364c72bb633aae5e141901
Source noteuspto-grants-2013_07