HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780955Generated: October 30, 2026
Methylparaben → 4-(2-Piperidinoethoxy)benzoic acid hydrochloride
https://huagongshe.com/reaction/1780955
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylparaben | HCID 7456 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidine, 1-(2-chloroethyl)-, hydrochloride | HCID 74826 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Piperidinoethoxy)benzoic acid hydrochloride | HCID 5743835 | — |
Reaction Steps
To a 250 mL 3 neck flask with mechanical stirring and condenser, and a heating apparatus consisting of an RTD probe in the flask hooked via a temperature controller to a heating mantle and under nitrogen atmosphere, the following was added: 7.61 g of methyl 4-hydroxybenzoate, 11.05 g of β-chloroethylpiperidine hydrochloride, 16.59 g of powdered potassium carbonate and 60 mL of ethyl acetate. The mixture was heated slowly to reflux. After overnight reflux, the mixture was cooled to ambient temperature, after which 60 mL of deionized water was added. The aqueous layer was separated and discarded. The organic layer was extracted with 4N hydrochloride (3 aliquots of 20 mL). The combined acid extracts were heated to reflux. After 1 hour at reflux, HPLC indicated the saponification to be 60% complete. After 4 hours, the reaction was near 100% complete. The mixture was cooled to 0° C.-5° C. and stirred. The resulting crystals were filtered, rinsed with acetone and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05631369 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-eb82cfb403a14a159e26a2010c1cf21e |
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| Source note | uspto-grants-1997_05 |
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