Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993328Generated: October 25, 2026

Methyl Ethyl Ketone → Ethyl 4-(2-Piperidinoethoxy)benzoate

https://huagongshe.com/reaction/993328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantEthylparabenHCID 8434—
ReactantPotassium CarbonateHCID 11430—
ReactantPiperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
SolventWaterHCID 962—
SolventEthyl acetate acetonitrile triethylamineHCID 86586431—
ProductEthyl 4-(2-Piperidinoethoxy)benzoateHCID 9838504—

Reaction Conditions

Temperature80 °C

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 monohydrochloride (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472531B1
Source datasetuspto-grants-2002_10
ORD IDord-0ce297b261d74b3d9e058303500aa2d3
Source noteuspto-grants-2002_10