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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613657Generated: October 30, 2026

Benzaldehyde → 2-Benzylaminomethyl-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/1613657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1,2,3,4-Tetrahydronaphthalen-2-ylmethanamineHCID 15718632—
SolventMethanolHCID 887—
Product2-Benzylaminomethyl-1,2,3,4-tetrahydronaphthaleneHCID 19774268—

Reaction Steps

A solution of 2-aminomethyl-1,2,3,4-tetrahydronaphthalene (XXXI) (14.5 g), benzaldehyde (9.7 g) and NaBH3CN (5.8 g) in methanol (150 ml) was cooled to 0°. Concentrated HCl was added dropwise until the apparent pH (litmus) was 3-4. The mixture was then stirred 16 hours at 0°. The solvent was evaporated, and the residue was dissolved in EtOAc, which was washed with saturated NaHCO3 solution, dried (MgSO4), and evaporated. The residual oil was dissolved in MeOH, and a slight excess of concentrated HCl was added. Adding EtOAc and boiling caused precipitation of Compound XXXIV.HCl, which was collected by filtration. Its NMR was consistent with the structure indicated, and it was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194450
Source datasetuspto-grants-1993_03
ORD IDord-e7802faec47a4369aa556e84058164ff
Source noteuspto-grants-1993_03