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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1154728Erstellt: 24. Oktober 2026

Methanol → Benzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)-

https://huagongshe.com/de/reaction/1154728

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt1-(4-Methoxyphenyl)-4-(4-nitrophenyl)piperazineHCID 5134657—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzenamine, 4-(4-(4-methoxyphenyl)-1-piperazinyl)-HCID 15440674%

Reaktionsschritte

A mixture of 12 parts of 1-(4-methoxyphenyl)-4-(4-nitrophenyl)piperazine, 200 parts of methanol and 225 parts of tetrahydrofuran is hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and washed with N,N-dimethylacetamide. The filtrate is poured onto water. The precipitated product is filtered off and crystallized from 1-butanol, yielding 8 parts (74%) of 4-[4-(4-methoxyphenyl)-1-piperazinyl]benzenamine; mp. 191.8° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04490530
Quelldatensatzuspto-grants-1984_12
ORD IDord-25c3423e6e894d7bb0b00ccbd2a57ac2
Quellennotizuspto-grants-1984_12