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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1352Erstellt: 23. Oktober 2026

Water → 1-Phenylcyclopentanecarboxylic acid

https://huagongshe.com/de/reaction/1352

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1,4-DibromobutaneHCID 8056—
EduktPhenylacetonitrileHCID 8794—
EduktEthyl AcetateHCID 8857—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium hydrideHCID 24758—
Produkt1-Phenylcyclopentanecarboxylic acidHCID 66167—

Reaktionsschritte

In a stream of argon, 60% sodium hydride was dissolved in 10 ml of tetrahydrofuran, and the solution was mixed with 2.0 g of benzyl cyanide, stirred for 1 hour at room temperature, further mixed with 3.69 g of 1,4-dibromobutane and again stirred for 16 hours at room temperature. The reaction mixture was mixed with water and ethyl acetate, and the resulting organic layer was separated, washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. After removing the solvent by distillation under a reduced pressure, the thus obtained residue was subjected to silica gel column chromatography, and the resulting hexane eluate was mixed with 45 ml of sulfuric acid and subjected to 24 hours of heating under reflux. After cooling down to room temperature, the reaction solution was mixed with ice water and ethyl acetate to separate water layer which was subsequently mixed with concentrated hydrochloric acid and ethyl acetate, and the resulting organic layer was separated, washed with water and a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. By removing the solvent by distillation under a reduced pressure, 978 mg of 1-phenylcyclopentanecarboxylic acid was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723606
Quelldatensatzuspto-grants-1998_03
ORD IDord-d699a2fd0bfb49f2b2d9d51a6a3e6ab2
Quellennotizuspto-grants-1998_03