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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 262012Erstellt: 24. Oktober 2026

2-Nitrophenol → 1-(Cyclopentyloxy)-2-nitrobenzene

https://huagongshe.com/de/reaction/262012

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-NitrophenolHCID 6947—
EduktBromocyclopentaneHCID 8728—
EduktPotassium CarbonateHCID 11430—
LösungsmittelAcetoneHCID 180—
Produkt1-(Cyclopentyloxy)-2-nitrobenzeneHCID 2216447346,8%

Reaktionsschritte

2-Nitrophenol (83.5 g, 0.60 mole), cyclopentyl bromide (98.0 g, 0.66 mole), anhydrous potassium carbonate (82.9 g, 0.60 mole) and dry acetone (600 cc) were refluxed for 72 hrs., and filtered to remove the potassium bromide. The residue was washed with acetone and the solvent was removed by rotary evaporation. The residue was partitioned between 200 cc of dichloromethane and water. The dichloromethane layer was washed with 200 cc of 10% potassium hydroxide, separated and the solvent was removed by rotary evaporation. The crude product was fractionally distilled at 144°-146° C. at 1.0 mm. Hg to yield 58.2 g of product (46.8%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04153446
Quelldatensatzuspto-grants-1979_05
ORD IDord-9cc3f965c1b640e1b7d43fc85411ead5
Quellennotizuspto-grants-1979_05