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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1005000Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/1005000

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromomethylnaphthaleneHCID 70320—
EduktTert-butyl 3-hydroxy-4-(4-methoxycarbonylphenyl)piperidine-1-carboxylateHCID 53949513—
Produkttert-butyl (3RS,4RS)-4-(4-methoxycarbonyl-phenyl)-3-naphthalen-2-ylmethoxy-piperidine-1-carboxylateHCID 54007898—

Reaktionsschritte

In an analogous manner to that described in Example 22(i), by alkylating tert-butyl (3RS,4RS)-3-hydroxy-4-(4-methoxycarbonyl-phenyl)-piperidine-1-carboxylate with 2-bromomethylnaphthalene there was obtained tert-butyl (3RS,4RS)-4-(4-methoxycarbonyl-phenyl)-3-naphthalen-2-ylmethoxy-piperidine-1-carboxylate as a colourless oil; MS: 476 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06051712
Quelldatensatzuspto-grants-2000_04
ORD IDord-68a30729bc524ff39648d2082a689383
Quellennotizuspto-grants-2000_04