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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414177Generated: October 31, 2026

1-Tetralone → 1-(Aminomethyl)-1,2,3,4-tetrahydronaphthalen-1-ol

https://huagongshe.com/reaction/414177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-TetraloneHCID 10724—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantLithiumHCID 3028194—
Catalystzinc(II)iodideHCID 9883512—
SolventTetrahydrofuranHCID 8028—
Product1-(Aminomethyl)-1,2,3,4-tetrahydronaphthalen-1-olHCID 1291485973%

Reaction Steps

Five and one-half g of trimethylsilylcyanide is added to a mixture of 7.3 g of 1-tetralone and 10 mg of zinc iodide. The mixture is stirred at room temperature overnight. It is dissolved in 25 ml dry THF and slowly added to a suspension of 2.3 g of lithium aluminumhydride in 40 ml of THF. Reaction is refluxed for three hours and upon cooling, carefully quenched with water. Precipitate is filtered and aqueous solution is diluted with 100 ml 1N NaOH. It was extracted with ether (3×100 ml), dried over anhydrous MgSO4, filtered, and ether evaporated yielding an oil which solidifies upon standing giving 6.4 g (73%) of (1-hydroxy-1,2,3,4-tetrahydronaphthyl)methylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04791103
Source datasetuspto-grants-1988_12
ORD IDord-329f329a0cdd4493b7078fea42a259cc
Source noteuspto-grants-1988_12