Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257289Erstellt: 25. Oktober 2026

Acetic Acid → 4-(Acetyloxy)-3-tert-butylbenzoic acid

https://huagongshe.com/reaction/257289

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktOxygenHCID 977—
EduktAcetic AnhydrideHCID 7918—
Edukt2-tert-Butyl-4-methylphenolHCID 17004—
KatalysatorHydrogen BromideHCID 260—
KatalysatorCobalt diacetateHCID 6277—
KatalysatorManganese dibromideHCID 6432071—
Produkt4-(Acetyloxy)-3-tert-butylbenzoic acidHCID 1800773684,4%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 82.0 g of 2-tert-butyl-4-methylphenol, 140.0 g of acetic anhydride and 3.0 g of hydrobromic acid (48%) is heated at 90° C. for 1 hour. 280.0 g of acetic acid, 2.5 g of cobalt(II) acetate (tetrahydrate) and 2.5 g of manganese(II) bromide (tetrahydrate) are added, and oxygen (30 ml/min) is passed through the solution at 110° C. The acetic acid is partially removed by applying a vacuum. The reaction mixture which remains is poured into 500 ml of water and filtered, giving 99.5 g (84%) of the product in the form of colourless crystals having a melting point of from 180° to 182° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05261953
Quelldatensatzuspto-grants-1993_11
ORD IDord-27fce9cf87e94677ab6c77efa7f38b23
Quellennotizuspto-grants-1993_11