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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27964Erstellt: 24. Oktober 2026

Hydrochloric Acid → gamma-(9,10-Dihydro-9,10-methano-9-anthryl)-beta-butenoic acid

https://huagongshe.com/de/reaction/27964

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethyl SulfoxideHCID 679—
EduktSodium hydrideHCID 24758—
Edukt(2-Carboxyethyl)triphenylphosphonium chlorideHCID 10270534—
Edukt9,10-Methanoanthracene-9(10H)-carbaldehydeHCID 12404141—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produktgamma-(9,10-Dihydro-9,10-methano-9-anthryl)-beta-butenoic acidHCID 54474651—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a mixture of 9-formyl-9,10-dihydro-9,10-methanoanthracene (110 mg) and β-carboxyethyltriphenylphosphonium chloride (186 mg) in dimethylsulfoxide (2 ml) and tetrahydrofuran (2 ml) was added 65.4% sodium hydride dispersion in mineral oil (37 mg) at 0° C. under nitrogen. The reaction mixture was stirred at 0° C. for 6 hours, diluted with water, acidified with hydrochloric acid and extracted with benzene. The benzene extract was shaken with 2 N aqueous sodium hydroxide. The basic layer was acidified with hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried over anhydrous sodium sulfate and evaporated to dryness to give γ-(9,10-dihydro-9,10-methano-9-anthryl)-β-butenoic acid. M.P. 166°-167° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04224344
Quelldatensatzuspto-grants-1980_09
ORD IDord-6a1bcab99e7646dca3cfbb7012c89a4b
Quellennotizuspto-grants-1980_09