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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165178Generated: October 30, 2026

Methylparaben → 4-(4-(1,1,3-Trimethyl-2-cyclohexyl)-butoxy)-benzoic acid methyl ester

https://huagongshe.com/reaction/2165178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylparabenHCID 7456—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium MethoxideHCID 10942334—
Reactant4-(1,1,3-Trimethyl-2-cyclohexyl)-2-butyl chlorideHCID 14457490—
CatalystTetrabutylammonium IodideHCID 67553—
SolventMethanolHCID 887—
Product4-(4-(1,1,3-Trimethyl-2-cyclohexyl)-butoxy)-benzoic acid methyl esterHCID 57234684—

Reaction Steps

Methanol was removed by distillation from a mixture of 11.7 g (77 mmol) 4-hydroxybenzoic acid methyl ester, 200 ml N-methylpyrrolidone, and I3.8 g (77 mmol) 30% sodium methylate solution in methanol, then 0.6 g tetrabutylammonium iodide and 20.0 g (92 mmol) 4-(1,1,3-trimethyl-2-cyclohexyl)-2-butyl chloride were added. This was followed by heating with stirring for 8 hours to 160° C. After cooling to room temperature, the reacted solution was filtered off from the sodium chloride formed, concentrated to dryness under reduced pressure, the evaporation residue was taken up in methylene chloride, washed with water, dried with sodium sulfate and, after concentration by evaporation, chromatographed on silica gel (Merck) (eluent: methylene chloride/toluene 7:3). 13.9 g (54% of the theoretical) of 4-(4-(1,1,3-trimethyl-2-cyclohexyl)-butoxy)-benzoic acid methyl ester were obtained in the form of a colorless oil having a refractive index at 20° C. of 1.5197.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939171
Source datasetuspto-grants-1990_07
ORD IDord-318b012a7c91428b80ce5c49e8b3d042
Source noteuspto-grants-1990_07