Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50864Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/50864

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl Ethyl KetoneHCID 6569—
EduktEthylparabenHCID 8434—
EduktPotassium CarbonateHCID 11430—
EduktPiperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl acetate acetonitrile triethylamineHCID 86586431—
ProduktEthyl 4-(2-Piperidinoethoxy)benzoateHCID 9838504—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

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 are added until the starting 4-hydroxybenzoate ester is 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713494B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-ae3cb0dae3e944c48580e55737574b4a
Quellennotizuspto-grants-2004_03