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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274641Generated: October 29, 2026

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

https://huagongshe.com/reaction/2274641

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 numberUS09126981B2
Source datasetuspto-grants-2015_09
ORD IDord-58578162ea4d49979df83f8bfa6d7add
Source noteuspto-grants-2015_09