Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 253386Erstellt: 25. Oktober 2026

1-(Bromomethyl)-4-chlorobenzene → 4-((4-Chlorobenzyl)oxy)-3-fluorobenzaldehyde

https://huagongshe.com/reaction/253386

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
Edukt3-Fluoro-4-hydroxybenzaldehydeHCID 587250—
Produkt4-((4-Chlorobenzyl)oxy)-3-fluorobenzaldehydeHCID 58086330—

Reaktionsschritte

Additional aldehydes were prepared using the protocol of Scheme 14, replacing either 4-chlorobenzyl bromide 22 with a suitable alkylating agent, and/or 3-fluoro-4-hydroxy-benzaldehyde 44 with a suitable aldehyde. The following table indicates the alkylating agent (column 1) and the starting aldehyde (column 2) used to afford the aldehyde (column 3) synthesized following this protocol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07872018B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-01feada5059d43139e39529df3f2287c
Quellennotizuspto-grants-2011_01