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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1004972Erstellt: 24. Oktober 2026

2-Bromomethylnaphthalene → tert-butyl (3RS,4RS)-4-(4-cyano-phenyl)-3-(naphthalen-2-ylmethoxy)-piperidine-1-carboxylate

https://huagongshe.com/de/reaction/1004972

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromomethylnaphthaleneHCID 70320—
Edukttert-butyl (3RS,4RS)-4-(4-cyano-phenyl)-3-hydroxy-piperidine-1-carboxylateHCID 54237291—
Produkttert-butyl (3RS,4RS)-4-(4-cyano-phenyl)-3-(naphthalen-2-ylmethoxy)-piperidine-1-carboxylateHCID 86604393—

Reaktionsschritte

In analogy to the procedure described in Example 1(g), by alkylating tert-butyl (3RS,4RS)-4-(4-cyano-phenyl)-3-hydroxy-piperidine-1-carboxylate with 2-bromomethyinaphthalene there was obtained tert-butyl (3RS,4RS)-4-(4-cyano-phenyl)-3-(naphthalen-2-ylmethoxy)-piperidine-1-carboxylate as a light yellow resin; MS: 443 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06051712
Quelldatensatzuspto-grants-2000_04
ORD IDord-102ea981ae964b24804ee2b7e91188ae
Quellennotizuspto-grants-2000_04