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HRID 247462Erstellt: 24. Oktober 2026

Water → 2-[(7-Methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochloride

https://huagongshe.com/de/reaction/247462

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPhenylglyoxalHCID 14090—
EduktSodium borohydrideHCID 4311764—
Edukt7-Methoxy-1,2,3,4-tetrahydronaphthalen-2-amine hydrochlorideHCID 14750915—
LösungsmittelMethanolHCID 887—
Produkt2-[(7-Methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochlorideHCID 2016088520%

Reaktionsbedingungen

Temperatur4 °C

Reaktionsschritte

An amount of 3.53 g of phenylglyoxal is reacted under stirring at room temperature for 3 hours with 5 g of 2-amino-7-methoxy-1,2,3,4-tetrahydronaphthalene hydrochloride in 100 ml of methanol in the presence of 0.9 g of sodium borohydride. After cooling to 4° C., 4,3 g of sodium borohydride are added and the reacting mixture is left under stirring at room temperature for a night. After addition of 20 ml of water, the solution is stirred at room temperature for 15 minutes, then it is evaporated to dryness. The residue is dissolved in 300 ml of ethyl acetate and 60 ml of water; after filtration, the organic phase is separated, dried over magnesium sulfate, filtered and evaporated to dryness. The oil thus obtained is purified by flash-chromatography by using a mixture ethyl acetate/methanol 8/2 as eluant to obtain the 2-[(7-methoxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol hydrochloride. Yield: 20% of the theoretical value.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04707497
Quelldatensatzuspto-grants-1987_11
ORD IDord-a395cc8371f745c7a98988b156bd69c4
Quellennotizuspto-grants-1987_11