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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 579781Erstellt: 26. Oktober 2026

Methanol → Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/579781

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktEthyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylateHCID 22708806—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelAcetic AcidHCID 176—
ProduktEthyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylateHCID 14049029—

Reaktionsschritte

A mixture of 73 parts of ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate, 400 parts of methanol and 150 parts of acetic acid was hydrogenated in the Parr-apparatus with 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. To the residue was added crushed ice and the whole was alkalized with potassium hydroxide. The aqueous phase was salted out with potassium carbonate and the product was extracted with benzene. The extract was dried, filtered and evaporated, yielding 63.5 parts of ethyl 4-(aminomethyl)-4-hydroxy-1-piperidinecarboxylate; mp. ±82° C. (intermediate 6).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04749702
Quelldatensatzuspto-grants-1988_06
ORD IDord-57e94454633f4bb884ce95040a1c1a8f
Quellennotizuspto-grants-1988_06