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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Oxabicyclo[3.1.0]hexaneHCID 9244—
EduktSodium hydrideHCID 24758—
Edukt6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazineHCID 10535622—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazineHCID 19934564—

Reaktionsbedingungen

Temperatur70 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420126
Quelldatensatzuspto-grants-1995_05
ORD IDord-658be5a07e2c441eb1bd87c04cd5b359
Quellennotizuspto-grants-1995_05