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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248805Generated: October 27, 2026

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

https://huagongshe.com/reaction/248805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
Reactant4-NitrobenzaldehydeHCID 541—
Reactant5-Bromo-2-hydroxybenzyl alcoholHCID 75342—
SolventEthyl AcetateHCID 8857—
Product6-Bromo-2-(4-nitrophenyl)-1,3-benzodioxanHCID 1896119570%

Reaction Conditions

Temperature5 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212171
Source datasetuspto-grants-1993_05
ORD IDord-246961ac753c41a7b1297a7ca94aeffc
Source noteuspto-grants-1993_05