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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248805Erstellt: 26. Oktober 2026

Benzoic Acid → 6-Bromo-2-(4-nitrophenyl)-1,3-benzodioxan

https://huagongshe.com/reaction/248805

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoic AcidHCID 243—
Edukt4-NitrobenzaldehydeHCID 541—
Edukt5-Bromo-2-hydroxybenzyl alcoholHCID 75342—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-Bromo-2-(4-nitrophenyl)-1,3-benzodioxanHCID 1896119570%

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

An intimately ground mixture of 5-bromo-2hydroxybenzyl alcohol (4.06 g), 4-nitrobenzaldehyde (3.93 g) and benzoic acid (0.2 g) was stirred and heated to 85° C. (±5° C.) under nitrogen for 88 hours. The clear melt which formed initially gradually solidified throughout the reaction period. The resulting solidified mass was cooled and dissolved in ethyl acetate (250 ml). The solution was then washed with 20% aqueous sodium carbonate, 20% aqueous sodium bisulphite and finally with brine. After drying over sodium sulphate, the organic phase was evaporated to yield a solid residue which was purified by briefly suspending in hot ethanol (approx. 75 ml) and cooling to 0°-5° C. The pure product was obtained as pale buff-coloured crystals (4.69g, 70%), mp 163°-164° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05212171
Quelldatensatzuspto-grants-1993_05
ORD IDord-246961ac753c41a7b1297a7ca94aeffc
Quellennotizuspto-grants-1993_05