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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzoic Acid | HCID 243 | — |
| Edukt | 4-Nitrobenzaldehyde | HCID 541 | — |
| Edukt | 5-Bromo-2-hydroxybenzyl alcohol | HCID 75342 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 6-Bromo-2-(4-nitrophenyl)-1,3-benzodioxan | HCID 18961195 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05212171 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-246961ac753c41a7b1297a7ca94aeffc |
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| Quellennotiz | uspto-grants-1993_05 |
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