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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 908092Erstellt: 24. Oktober 2026

P-Chloroacetophenone → p-Chlorophenacyl bromide

https://huagongshe.com/de/reaction/908092

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktP-ChloroacetophenoneHCID 7467—
LösungsmittelAcetic AcidHCID 176—
Produktp-Chlorophenacyl bromideHCID 68303—
Produkt2-Amino-1-(4-chlorophenyl)ethan-1-one hydrochlorideHCID 2798211—

Reaktionsschritte

The starting 2-amino-1-(4-chlorophenyl)ethanone hydrochloride was prepared according to the following procedure. The 1-(4-chlorophenyl)ethanone (1.0 eq.) was dissolved in glacial acetic acid (1 ml, per mmol). To this was added a slurry of pyridinium bromide perbromide (1.03 eq.) in acetic acid (1 mL per mmol). The heterogeneous mixture was stirred for 4 h at ambient temperature. After about 30 min. the mixture turned homogeneous. After pouring into ice-water a yellow precipitate was filtered off and washed with water (2×1 mL per mmol of starting ketone). Drying of the precipitate afforded 2-bromo-1-(4-chlorophenyl)ethanone in ca. 90% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08017555B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-c36b39ac91384ba699e4e403ccd48175
Quellennotizuspto-grants-2011_09