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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1916261Erstellt: 24. Oktober 2026

Acetic Acid → 2-(4-Chlorophenyl)-4,5-dimethyl-1,3-oxazol 3-oxide

https://huagongshe.com/de/reaction/1916261

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
Edukt4-ChlorobenzaldehydeHCID 7726—
Edukt2,3-Butanedione monoximeHCID 6409633—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-(4-Chlorophenyl)-4,5-dimethyl-1,3-oxazol 3-oxideHCID 3243952—

Reaktionsschritte

1.00 g (9.89 mmol) of diacetyl monoxime and 1.53 g (10.88 mmol) of 4-chlorobenzaldehyde were initially charged in 2 ml (34.94 mmol) of glacial acetic acid. Then, while the reaction mixture was cooled with ice, hydrogen chloride gas was introduced for 30 min. 10 ml of diethyl ether were then added to the reaction mixture. A precipitate was formed which was filtered off and washed twice with in each case 2 ml of diethyl ether. The precipitate was resuspended in about 5 ml of water and the suspension was made basic using 25% strength aqueous ammonia solution. The mixture was extracted four times with in each case 10 ml of dichloromethane. The combined organic phases were dried over magnesium sulfate and the solvent was removed on a rotary evaporator. Without further purification, the residue was used for the next reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08618119B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-c5115581a6af491e8b88c977cca06d60
Quellennotizuspto-grants-2013_12