HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131587Erstellt: 26. Oktober 2026
Hydrochloric Acid → 4-Cyclopentyloxy-3-hydroxybenzaldehyde
https://huagongshe.com/reaction/131587
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Bromocyclopentane | HCID 8728 | — |
| Edukt | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Cyclopentyloxy-3-hydroxybenzaldehyde | HCID 16726149 | 67% |
Reaktionsschritte
A suspension of 3,4-dihydroxybenzaldehyde (5.0 gm, 0.0362 mol), anhydrous potassium carbonate (6.0 gm, 0.0434 mol) and cyclopentyl bromide (6.5 gm, 0.0434 mol) in dry DMF (50 ml) was heated and stirred at 80° C. for 24 hrs. Reaction mixture was then cooled and diluted with water (500 ml), acidified with 1N HCl and extracted with ethyl acetate (3×100 ml). The ethyl acetate extract was washed 5% sodium bicarbonate and brine and dried over anhydrous sodium sulfate. The dried extract on concentration afforded a residue which was purified by silica gel chromatography using 10% ethyl acetate in petroleum ether as the eluent to provide 5.0 gm of the title product as white solid. mp: 87-89° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07384962B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-090b96ab78684a2ba796cb9117c35e13 |
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| Quellennotiz | uspto-grants-2008_06 |
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