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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 327756Erstellt: 24. Oktober 2026

Phenacyl bromide → Ethanone, 2-(acetyloxy)-1-phenyl-

https://huagongshe.com/de/reaction/327756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenacyl bromideHCID 6259—
EduktAcetic AnhydrideHCID 7918—
EduktSodium AcetateHCID 517045—
LösungsmittelAcetic AcidHCID 176—
ProduktEthanone, 2-(acetyloxy)-1-phenyl-HCID 222851—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of 2-bromoacetophenone (199 g, 1.0M), acetic acid (200 mL) and acetic anhydride (30 mL) was stirred and heated to about 60° C. Anhydrous sodium acetate (100 g, 1.2M) was added and the reaction mixture was heated and stirred at about 130° C. for 6.0 hrs and then allowed to cool. To remove most of the salt, the reaction mixture was filtered through a sintered glass funnel. The acetic acid and acetic anhydride were removed from the filtrate using a rotary evaporator. A white solid was obtained upon cooling (yield--97.0 g). Mass spectroscopy supported the proposed structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05274072
Quelldatensatzuspto-grants-1993_12
ORD IDord-013b7c690e714cb1b9f2dbb4d4b29262
Quellennotizuspto-grants-1993_12