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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylparaben | HCID 7456 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-(1,1,3-Trimethyl-2-cyclohexyl)-2-butyl chloride | HCID 14457490 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(4-(1,1,3-Trimethyl-2-cyclohexyl)-butoxy)-benzoic acid methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04939171 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-318b012a7c91428b80ce5c49e8b3d042 |
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| Source note | uspto-grants-1990_07 |
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