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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274637Generated: November 1, 2026

1-Naphthaldehyde → HCID 53411263, compound

https://huagongshe.com/reaction/2274637

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
Reactant2,2-DiethoxyethylamineHCID 69524—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 53411263HCID 5341126368.6%

Reaction Steps

To a solution of 1-naphthaldehyde (2.2 ml, 16.0 mmol) in tetrahydrofuran (6 ml) was added 2,2-diethoxyethanamine (2.9 ml, 20.0 mmol) and the mixture was stirred at room temperature 0.5 hr. And then sodium triacetoxyborohydride (10.6 g, 50 mmol) was added and the mixture was stirred for additional 4 hr. The reaction mixture was diluted with ethyl acetate (200 ml) and washed with saturated aqueous sodium bicarbonate (200 ml), water (200 ml) and brine (200 ml). The organic layer was dried over magnesium sulfate (5 g) and filtered. The filtrate was concentrated in vacuo and the residue was purified by silica gel column chromatography (eluent: n-hexane:ethyl acetate=100:0 to 70:30) to obtain the title compound (3.0 g, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126981B2
Source datasetuspto-grants-2015_09
ORD IDord-400204c8f1db4402b3fc50808d4f3666
Source noteuspto-grants-2015_09