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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708172Generated: November 1, 2026

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

https://huagongshe.com/reaction/1708172

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-2-hydroxybenzyl 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 (4.69 g, 70%), mp 163°-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356924
Source datasetuspto-grants-1994_10
ORD IDord-37ace0a8a9c845ef83107d17ad4f4934
Source noteuspto-grants-1994_10