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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414693Erstellt: 23. Oktober 2026

Hydrochloric Acid → 1-n-Butylamino-4,6-dimethyl-7-hydroxyindane hydrochloride

https://huagongshe.com/de/reaction/414693

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktButylamineHCID 8007—
Edukt4,6-Dimethyl-7-hydroxy-1-indanoneHCID 240718—
EduktSodium AcetateHCID 517045—
EduktSodium borohydrideHCID 4311764—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt1-n-Butylamino-4,6-dimethyl-7-hydroxyindane hydrochlorideHCID 13604203—

Reaktionsschritte

100 Milliliters of ethanol solution containing 1.76 g of 4,6-dimethyl-7-hydroxy-1-indanone and 14.6 g of n-butylamine was refluxed by heating for 8 hours. The reaction mixture was cooled to a room temperature, then 1.0 g of sodium borohydride was added thereto. The mixture was further stirred at a room temperature for 1 hour. The reaction mixture was concentrated to dryness and the residue obtained was dissolved in 100 ml of water. Then the solution was acidified by adding a concentrated hydrochloric acid, and the pH of the solution was adjusted to about pH=9 by adding a saturated sodium acetate aqueous solution. The precipitate formed was extracted with ethyl acetate, washed with water and dried. The solvent was removed by evaporation, the residue obtained was dissolved in 100 ml of ethanol, and changed to hydrochloride by adding ethanol being saturated with hydrogen chloride gas. Recrystallized from ethanol-ether to obtain 1.89 g of 1-n-butylamino-4,6-dimethyl-7-hydroxyindane hydrochloride in the form of colorless needle-liee crystals. Melting point: 143°-144° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04792628
Quelldatensatzuspto-grants-1988_12
ORD IDord-a57bc510ba94475d92c3cf9b77a8736b
Quellennotizuspto-grants-1988_12