HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 457503Erstellt: 26. Oktober 2026
4-Hydroxybenzaldehyde → 4-Cyclobutoxybenzaldehyde
https://huagongshe.com/reaction/457503
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Bromocyclobutane | HCID 78110 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Cyclobutoxybenzaldehyde | HCID 21989708 | 75,1% |
Reaktionsschritte
To a suspension of 4-hydroxybenzaldehyde (0.12 g) and cesium carbonate (0.49 g) in N,N-dimethylformamide (2 mL) was added cyclobutyl bromide (0.15 g), and the mixture was stirred at 65° C. overnight. To the reaction mixture was added 1 mol/L aqueous sodium hydroxide solution, and the mixture was extracted with diethyl ether. The organic layer was washed with 0.5 mol/L aqueous sodium hydroxide solution, water and brine, and dried over an hydrous magnesium sulfate. The solvent was removed under reduced pressure to give 4-cyclobutyloxybenzaldehyde (0.13 g). To a solution of the obtained 4-cyclobutyloxybenzaldehyde (0.13 g) in methanol (10 mL) was added sodium borohydride (0.056 g), and the mixture was stirred at room temperature overnight. To the reaction mixture was added 1 mol/L hydrochloric acid solution, and the mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to give 4-cyclobutyloxybenzyl alcohol (0.12 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07189702B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-dc01b6c49a9841ca83bca78b91365ffa |
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| Quellennotiz | uspto-grants-2007_03 |
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