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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1764644Erstellt: 26. Oktober 2026

Chlorobenzene → 4-(4-Chlorophenyl)-2-methyl-4-oxobutanoic acid

https://huagongshe.com/reaction/1764644

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorobenzeneHCID 7964—
EduktMethylsuccinic anhydrideHCID 20051—
EduktAluminum(III) ChlorideHCID 6451240—
Produkt4-(4-Chlorophenyl)-2-methyl-4-oxobutanoic acidHCID 2733715—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a solution of 114 g. of methylsuccinic anhydride in 400 ml. of chlorobenzene is added carefully 270 g. of aluminum chloride. The mixture is heated to 65° C. for 11/2 hours, is cooled, quenched with ice and concentrated hydrochloric acid and extracted with benzene. The benzene layer is extracted with aqueous sodium bicarbonate. After adjusting the pH of the bicarbonate solution to 6.3, concentrated hydrochloric acid is added slowly over a period of several hours with stirring. At pH 5.7, 78 g. of white crystals are filtered off. Recrystallization of this material from ethanol-water affords 3-(p-chlorobenzoyl)-2-methylpropionic acid as white crystals. A mixture of 35.50 g. of the preceding compound, 85 ml. of hydrazine hydrate and 400 ml. of ethyl alcohol is allowed to stir at reflux for 18 hours. The reaction mixture is concentrated to about 75% of the original volume, cooled in an ice bath and filtered to yield 26.62 g. of 6-(p-chlorophenyl)-4,5-dihydro-4-methyl-3(2H)-pyridazinone as a yellow solid. An additional 4.7 g. of product is obtained from the filtrate above.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04117130
Quelldatensatzuspto-grants-1978_09
ORD IDord-cab4969c458d4c51b0ed63328d8858ab
Quellennotizuspto-grants-1978_09