HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39332Erstellt: 24. Oktober 2026
Bromocyclopentane → 4-Cyclopentyloxy-3-hydroxybenzaldehyde
https://huagongshe.com/de/reaction/39332
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bromocyclopentane | HCID 8728 | — |
| Edukt | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Cyclopentyloxy-3-hydroxybenzaldehyde | HCID 16726149 | — |
Reaktionsschritte
A suspension of 3,4-dihydroxy benzaldehyde (50.0 g, 0.3623 mol), cyclopentyl bromide (135 g, 0.9058 mol) and potassium carbonate (50.0 g, 0.3623 mol) in N,N-dimethylformamide (500 mL) was stirred at about 75-80° C. for about 1.0 hr. 4×12.5 g potassium carbonate was then added after every 1.0 hr. The reaction mixture was cooled to ambient temperature and filtered to remove inorganic materials. The residue obtained after concentration of the filtrate was diluted with toluene (250 mL), and extracted with 5-10% aqueous sodium hydroxide solution (6×50 mL). The combined aqueous layer was acidified to pH about 3 to 5 by 5N aqueous hydrochloric acid solution. The solid which separated was filtered, washed with water and dried to give 4-cyclopentyloxy-3-hydroxy benzaldehyde.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524905B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-89aa6abc2ce546009d22bfdcfac4be8d |
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| Quellennotiz | uspto-grants-2013_09 |
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