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HRID 248805作成日:2026年10月27日

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

https://huagongshe.com/reaction/248805

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoic AcidHCID 243—
反応物4-NitrobenzaldehydeHCID 541—
反応物5-Bromo-2-hydroxybenzyl alcoholHCID 75342—
溶媒Ethyl AcetateHCID 8857—
生成物6-Bromo-2-(4-nitrophenyl)-1,3-benzodioxanHCID 1896119570%

反応条件

温度5 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05212171
出典データセットuspto-grants-1993_05
ORD IDord-246961ac753c41a7b1297a7ca94aeffc
出典メモuspto-grants-1993_05