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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799245Generated: October 31, 2026

Methylparaben → Methyl 4-[2-(4-chlorophenyl)ethoxy]benzoate

https://huagongshe.com/reaction/1799245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylparabenHCID 7456—
ReactantPotassium CarbonateHCID 11430—
ReactantDimethylacetamideHCID 31374—
Reactant2-(4-Chlorophenyl)ethyl 4-methylbenzenesulfonateHCID 244773—
SolventWaterHCID 962—
ProductMethyl 4-[2-(4-chlorophenyl)ethoxy]benzoateHCID 6901733890.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

Potassium carbonate (54.9 g, 397 mmol) was added to a N,N-dimethylacetamide (330 mL) solution of methyl 4-hydroxybenzoate (25.2 g, 165 mmol) and 2-(4-chlorophenyl)ethyl p-toluenesulfonate (compound described in J. Am. Chem. Soc., (1978), 100, 228-246, 61.7 g, 199 mmol) at room temperature. The mixture was stirred at 120° C. for 1.5 hours. The reaction solution was cooled to room temperature, and water (1 L) was added thereto. The resulting mixture was extracted with ethyl acetate three times. The organic layers were combined, washed with water (three times) and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate, 10:1, V/V) to give 43.2 g of methyl 4-[2-(4-chlorophenyl)ethoxy]benzoate (white solid). All this solid was dissolved in ethanol (430 mL), and a 2 M lithium hydroxide aqueous solution (148 mL, 297 mmol) was added thereto. The mixture was stirred at 60° C. for 2 hours, and the solvents (mainly ethanol) were evaporated. The residue was suspended in water (300 mL), and 2 N hydrochloric acid (160 mL) was added thereto under ice-cooling with stirring. The precipitated white solid was collected by filtration, washed with water and n-hexane, and dried under reduced pressure to give 41.0 g of the title compound (white solid, yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344029B2
Source datasetuspto-grants-2013_01
ORD IDord-d74dcd746dd94b91962a84ff8dbac9e5
Source noteuspto-grants-2013_01