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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 321917Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4,7-dimethyl-1H-indene

https://huagongshe.com/reaction/321917

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Eduktp-Toluenesulfonic acidHCID 6101—
EduktSodium SulfateHCID 24436—
Edukt4,7-Dimethyl-1-indanoneHCID 220094—
EduktSodium BicarbonateHCID 516892—
Edukt4,7-Dimethyl-1-indanolHCID 15877605—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4,7-dimethyl-1H-indeneHCID 8145891,9%

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

2.9 g (0.0181 moles) of 4,7-dimethyl-1-indanone (formula XVII) obtained as described above, are slowly added to a suspension of 0.350 g (0.0692 moles) of LiAlH4 in 30 ml of ethyl ether, maintained at −30° C. in an inert atmosphere. The reaction is complete after 30 minutes. Ice and HCl 2N are cautiously added until acidification, the mixture is then extracted with ethyl ether, and the organic phase is subsequently separated and washed until neutrality. It is anhydrified on sodium sulfate and evaporated, obtaining a residue essentially consisting of 4,7-dimethyl-1-indanol. The residue is dissolved in 10 ml of THF, a pinch of p-toluenesulfonic acid is added and the mixture is brought to reflux temperature for 1 hour. Solid NaHCO3 and Na2SO4 are then added. The mixture is filtered and the solvent evaporated obtaining 2.4 g of 4,7-dimethylindene (XVIII) (91% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211110B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-0aa9780815a7402c8577ecf3c21be3fa
Quellennotizuspto-grants-2001_04