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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 67884Erstellt: 24. Oktober 2026

3-Bromobenzaldehyde → 1-(3-Bromophenyl)-7-chloro-1-hepten-3-one

https://huagongshe.com/de/reaction/67884

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-BromobenzaldehydeHCID 76583—
Edukt[(tetrahydro-2H-pyran-2-ylidene)methyl]triphenylphosphonium chlorideHCID 73680070—
LösungsmittelO-XyleneHCID 7237—
Produkt1-(3-Bromophenyl)-7-chloro-1-hepten-3-oneHCID 54015826—

Reaktionsschritte

2 parts of [(tetrahydro-2H-pyran-2-ylidene)methyl] triphenylphosphonium chloride and 1.85 parts of 3-bromobenzaldehyde were combined in 45 parts of xylene. This was maintained under a nitrogen atmosphere and was refluxed for 3 hours. After the reaction mixture was cooled to room temperature, xylene was removed at a temperature of about 60° C. and under reduced pressure, leaving a product mixture. This mixture was separated chromatographically on a silica column using benzene as the elution solvent, to yield 1-(3-bromophenyl)-7-chloro-1-hepten-3-one.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04347192
Quelldatensatzuspto-grants-1982_08
ORD IDord-35f440df14024a91bd8fc301d5da4a63
Quellennotizuspto-grants-1982_08