HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2783Generated: October 23, 2026
Methyl Ethyl Ketone → Ethyl 4-(2-Piperidinoethoxy)benzoate
https://huagongshe.com/en/reaction/2783
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Ethylparaben | HCID 8434 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidine, 1-(2-chloroethyl)-, hydrochloride | HCID 74826 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl acetate acetonitrile triethylamine | HCID 86586431 | — |
| Product | Ethyl 4-(2-Piperidinoethoxy)benzoate | HCID 9838504 | — |
Reaction Steps
A mixture of ethyl 4-hydroxybenzoate (8.31 g), 1-(2-chloroethyl)piperidine monohydrochloride (10.13 g), potassium carbonate (16.59 g), and methyl ethyl ketone (60 mL) was heated to 80° C. After one hour, the mixture was cooled to about 55° C. and treated with additional 1-(2-chloroethyl)piperidine mono-hydrochloride (0.92 g). The resulting mixture was heated to 80° C. The reaction was monitored by thin layer chromatography (TLC), using silica-gel plates and ethyl acetate/acetonitrile/triethylamine (10:6:1, v/v). Additional portions of 1-(2-chloroethyl)piperidine hydrochloride were added until the starting 4-hydroxybenzoate ester was consumed. Upon complete reaction, the reaction mixture was treated with water (60 mL) and allowed to cool to room temperature. The aqueous layer was discarded and the organic layer concentrated in vacuo at 40° C. and 40 mm Hg. The resulting oil was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05731327 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-6f47bc261884491694bca9fab87d052d |
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| Source note | uspto-grants-1998_03 |
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