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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 361967Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/361967

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 waterand 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 ofthe 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 crystals are washed with petrolether andsucked off; 0.64 g (39% y), mp. 182° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05866722
Quelldatensatzuspto-grants-1999_02
ORD IDord-f2bc4d1e56aa4859abea606d965acb6e
Quellennotizuspto-grants-1999_02