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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63075Generated: October 26, 2026

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

https://huagongshe.com/reaction/63075

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-alpha-tetraloneHCID 14112—
ReactantSodium HydroxideHCID 14798—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantAluminium lithium hydrideHCID 21226445—
Catalystzinc(II)iodideHCID 9883512—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-olHCID 1319758968.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447045B2
Source datasetuspto-grants-2016_09
ORD IDord-060b901605a7488ead9bd01c7620fa71
Source noteuspto-grants-2016_09