Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Trityl-4-ethoxymethylpyrazole | HCID 68528513 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Acetone ethanol | HCID 21889777 | — |
| Produkt | 4-Ethoxymethylpyrazole | HCID 68532829 | 44% |
Reaktionsschritte
1-trityl-4-ethoxymethylpyrazole (1.800 g, 4.88 mmol) was dissolved in a mixture of ethanol/acetone (15 ml/5 ml) and 30 mL of 2N HCl was added to the resulting solution. The mixture was heated at 80° C. for 2 h. After cooling to room temperature, the reaction mixture was filtered and washed with dichloromethane. The aqueous layer was basified with 2N NaOH and extracted with dichloromethane. The organic layers were combined, dried over MgSO4 and the solvent was evaporated under vacuum yielding compound 4-ethoxymethylpyrazole as a white oil. Yield: 44% (270 mg, 2.14 mmol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08372379B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-0bea6f2677724088b732e77957c79f23 |
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| Quellennotiz | uspto-grants-2013_02 |
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