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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 345135Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/345135

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 pressude. 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
PatentnummerUS05055474
Quelldatensatzuspto-grants-1991_10
ORD IDord-4ccb95ee66a448edb815f76c73aeda7c
Quellennotizuspto-grants-1991_10