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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 965458Erstellt: 24. Oktober 2026

Acetic Acid → 2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenone

https://huagongshe.com/de/reaction/965458

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrogen BromideHCID 260—
Edukt2,6-Dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenoneHCID 22719953—
LösungsmittelWaterHCID 962—
Produkt2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenoneHCID 54569551—

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

A mixture of 2,6-dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenone (1.78 g; 5 mmol) hydrobromic acid (7.5 ml; 30% in acetic acid) and acetic acid (7.5 ml) is stirred at 75° C. for 2 hours. Water is added and the mixture extracted with methylenechloride. The extract is washed with water and shaken with 2N sodium hydroxide. The alcaline solution is acidified with hydrochloric acid, the separated compound dissolved in methylenechloride and the solution washed with water. After evaporation of the solvent purification is carried out by chromatography (flash column, filled with 36 g of silicagel; elution with 500 ml of petrolether/ethylacetate (4:1; v/v) and 250 ml of petrolether/ethylacetate (1:1; v/v)). the fraction containing the compound is concentrated, the compound crystallized. The yellow crystalls are washed with petrolether and sucked off; 0.64 g (39% y), mp. 182° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05773663
Quelldatensatzuspto-grants-1998_06
ORD IDord-e0902ff2670344b8a8a18cf4659cc88c
Quellennotizuspto-grants-1998_06