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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 330245Erstellt: 24. Oktober 2026

Sodium Bicarbonate → 1-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-indene

https://huagongshe.com/de/reaction/330245

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
Edukt2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-inden-1-one oximeHCID 136342832—
EduktHCID 178418361HCID 178418361—
KatalysatorPlatinum oxide (PtO)HCID 82844—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt1-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-indeneHCID 14030334—

Reaktionsschritte

3.00 Grams of 2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-inden-1-one oxime was dissolved in 55 ml of glacial acetic acid, and this solution was subjected to catalytic hydrogenation in the presence of 0.3 g of platinum oxide at room temperature under 4 atmospheric hydrogen gas pressure. The hydrogenation was terminated at the point when the stoichiometric amount of hydrogen was absorbed. The catalyst was removed by filtration and the filtrate thus obtained was concentrated. The residue thus obtained was dissolved in water and the pH of this solution was adjusted to about pH 8 by adding an aqueous solution of sodium bicarbonate, then extracted with 200 ml of chloroform. The chloroform extract was washed with water, dried with anhydrous magnesium sulfate, then concentrated under a reduced pressure. Recrystallized from ethanol to obtain 0.24 g of 1-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-indene. Colorless needle-like crystals. Melting point: 135°-136° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04895847
Quelldatensatzuspto-grants-1990_01
ORD IDord-ccdc767980c948329a7da75b51dc494d
Quellennotizuspto-grants-1990_01