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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 451589Erstellt: 24. Oktober 2026

Ammonia → 5-tert-butyl-2,3-dihydro-1H-inden-1-amine

https://huagongshe.com/de/reaction/451589

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
Edukt5-tert-butyl-1-indanone O-methyloximeHCID 73047460—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
Produkt5-tert-butyl-2,3-dihydro-1H-inden-1-amineHCID 11506601—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

5-tert-Butyl-1-indanone O-methyloxime (4.37 g, 20.2 mmol) and 10% palladium on carbon (2.2 g) were combined in methanol (50 ml) and ammonia (10 ml) and placed in a Parr apparatus, which was charged with hydrogen to 60 psi. The reaction was shaken at 50° C. for 16 hours. The reaction mixture was filtered and the filtrate was evaporated under reduced pressure. The residue was treated with diethyl ether (100 ml) and extracted with hydrochloric acid (1N, 3×50 ml). The combined aqueous extracts were neutralized with sodium hydroxide (6 g) in water (25 ml) and extracted with diethyl ether. The organic extracts were combined, dried with magnesium sulfate, and the filtrate was evaporated under reduced pressure to provide the title compound, which was used without further purification in the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08487116B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-9e243e9d9646465aaec0cc424959d5bf
Quellennotizuspto-grants-2013_07