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HRID 63075Erstellt: 24. Oktober 2026

6-Methoxy-alpha-tetralone → 1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol

https://huagongshe.com/de/reaction/63075

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Methoxy-alpha-tetraloneHCID 14112—
EduktSodium HydroxideHCID 14798—
EduktTrimethylsilyl cyanideHCID 82115—
EduktAluminium lithium hydrideHCID 21226445—
Katalysatorzinc(II)iodideHCID 9883512—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-olHCID 1319758968,4%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

TMS-cyanide (8.52 mL, 68.1 mmol) was added to a solution of 6-methoxy-1-tetralone (6.0 g, 34 mmol) in toluene (50 mL). A trace amount (˜20 mg) of zinc iodide was added, and the reaction was stirred at 60° C. for 16 hours. The solution was cooled to rt and diluted with THF (30 mL). This was added to a mixture of lithium aluminum hydride (2.58 g) in THF (50 mL), and the reaction mixture was heated at 42° C. for 2 h. The reaction was cooled to rt. EtOAc (10 mL) was slowly added, and the reaction stirred 30 min. Water (2 mL) and then 5N NaOH (1 mL) were slowly added, and the reaction stirred 1 h. The reaction mixture was diluted with EtOAc (100 mL), dried (MgSO4), and filtered through Celite. Purification by silica gel chromatography (10-20% MeOH/DCM) gave 4.82 g of 1-(aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol as a clear oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447045B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-060b901605a7488ead9bd01c7620fa71
Quellennotizuspto-grants-2016_09