HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34968Erstellt: 24. Oktober 2026
Tetrahydrofuran → 4-(2-Propyl-3,4-dichlorophenoxy)butane nitrile
https://huagongshe.com/de/reaction/34968
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 5-Bromopentanenitrile | HCID 79435 | — |
| Edukt | 3,4-Dichloro-2-propylphenol | HCID 600360 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Hexamethylphosphoramide | HCID 12679 | — |
| Produkt | 4-(2-Propyl-3,4-dichlorophenoxy)butane nitrile | HCID 21297293 | — |
Reaktionsschritte
To a solution of 37.1 g. of 2-propyl-3,4-dichlorophenol in 400 ml. of dry tetrahydrofuran and 25 ml. of hexamethylphosphoramide were added 32 ml. of 5-bromovaleronitrile. Sodium hydride (7.2 g. of a 60% dispersion in mineral oil) was added and the reaction was stirred for about three days at 65° C. The reaction mixture was cooled to room temperature and ethyl acetate and water were added. The solution was evaporated and ethyl acetate and water were added. The layers were separated and the ethyl acetate was washed several times with dilute hydrochlorid acid. The organic layer was filtered through sodium sulfate and evaporated to provide the desired nitrile intermediate. NMR.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04764521 |
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| Quelldatensatz | uspto-grants-1988_08 |
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| ORD ID | ord-926f1687b0174b80a0cedf65e944a367 |
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| Quellennotiz | uspto-grants-1988_08 |
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