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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361963Generated: October 29, 2026

1-Naphthaldehyde → (S)-1,1-diethoxy-N-(naphthalen-1-ylmethyl)propan-2-amine

https://huagongshe.com/reaction/2361963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(2S)-1,1-Diethoxy-2-propanamineHCID 12398111—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(S)-1,1-diethoxy-N-(naphthalen-1-ylmethyl)propan-2-amineHCID 6707519667.1%

Reaction Steps

To a solution of (S)-1,1-diethoxypropan-2-amine (Compound XVIII-1) (682 mg, 3.55 mmol) in tetrahydrofuran (2 ml) was added 1-naphthaldehyde (554 mg, 3.55 mmol) and the mixture was stirred at room temperature for 0.5 hr. The reaction mixture was diluted with tetrahydrofuran (3 ml) and sodium triacetoxyborohydride (829 mg, 3.91 mmol) was added and the mixture was stirred at room temperature for 18 hr. The reaction mixture was diluted with ethyl acetate (50 ml) and washed with saturated aqueous sodium bicarbonate (50 ml) twice, water (50 ml) twice and brine (50 ml) twice. The organic layer was dried over magnesium sulfate and filtered and the filtrate was concentrated in vacuo to obtain the title compound (685 mg, 67.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691819B2
Source datasetuspto-grants-2014_04
ORD IDord-5d25f412261b42f9996e61e6279297e9
Source noteuspto-grants-2014_04