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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 893829Erstellt: 24. Oktober 2026

Ethyl chloroformate → 4-(2,3,4-Trimethoxybenzylthio)-1-cinnamylpiperidine

https://huagongshe.com/de/reaction/893829

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl chloroformateHCID 10928—
EduktPotassium HydroxideHCID 14797—
EduktToluene, alpha-chloro-2,3,4-trimethoxy-HCID 97491—
EduktSodiumHCID 5360545—
EduktFumarateHCID 5460307—
Edukt1-Methylpiperidine-4-thiolHCID 14180391—
Edukt4-(2,3,4-Trimethoxybenzylthio)-1-ethoxycarbonylpiperidineHCID 19890907—
Edukt4-(2,3,4-Trimethoxybenzylthio)-1-cinnamylpiperidine fumarateHCID 67894540—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthanolHCID 702—
Produkt4-(2,3,4-Trimethoxybenzylthio)-1-cinnamylpiperidineHCID 53752093—

Reaktionsschritte

The 4-(2,3,4-trimethoxybenzylthio)piperidine used as starting material, the fumarate of which melts at 154° C., was prepared by the hydrolysis, using potassium hydroxide and ethanol, of 4-(2,3,4-trimethoxybenzylthio)-1-ethoxycarbonylpiperidine (oil), which was itself prepared by the action of ClCOOC2H5 in benzene on 4-(2,3,4-trimethoxybenzylthio)-1-methylpiperidine (m.p. of the corresponding fumarate: 130° C.), which was itself prepared by the condensation of 2,3,4-trimethoxybenzyl chloride in ethanol with the sodium salt of 1-methyl-4-mercaptopiperidine, b.p./13 : 70°-72° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05126356
Quelldatensatzuspto-grants-1992_06
ORD IDord-723d3b8048ee46d3b6b86ab349d9e5a4
Quellennotizuspto-grants-1992_06