HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37119Erstellt: 24. Oktober 2026
6-Oxabicyclo[3.1.0]hexane → 6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazine
https://huagongshe.com/de/reaction/37119
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 6-Oxabicyclo[3.1.0]hexane | HCID 9244 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazine | HCID 10535622 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazine | HCID 19934564 | — |
Reaktionsschritte
In 20 ml of N,N-dimethylformamide was dissolved 1.0 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazine followed by addition of 0.24 g of sodium hydride. The mixture was stirred at 70° C. for 1 hour and after cooling to room temperature, 0.5 ml of cyclopentene oxide was added. The mixture was stirred at 70° C. for 3 hours. The reaction mixture was then allowed to cool, diluted with water and extracted with ethyl acetate. The extract was washed with water and aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography and the resulting crude crystals were recrystallized from ethyl acetate-hexane to give 0.53 g of 6-cyano-3,4-dihydro-4-(2-hydroxycyclopentan-1-yl)-2,2-dimethyl-2H-1,4-benzoxazine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05420126 |
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| Quelldatensatz | uspto-grants-1995_05 |
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| ORD ID | ord-658be5a07e2c441eb1bd87c04cd5b359 |
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| Quellennotiz | uspto-grants-1995_05 |
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