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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981573Generated: October 30, 2026

Aminoacetaldehyde dimethyl acetal → N-(3,5-difluoro-4-methoxybenzyl)-aminoacetaldehyde dimethyl acetal

https://huagongshe.com/reaction/981573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantSodium borohydrideHCID 4311764—
Reactant3,5-Difluoro-4-methoxybenzaldehydeHCID 14450860—
SolventEthanolHCID 702—
ProductN-(3,5-difluoro-4-methoxybenzyl)-aminoacetaldehyde dimethyl acetalHCID 1445086296.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

3,5-Difluoro-4-methoxybenzaldehyde (3.38 g, 0.0196 mole) was added to aminoacetaldehyde dimethyl acetal (2.14 ml, 0.0196 mole) and the mixture was heated at 100° C. for 2 hours. The reaction mixture was cooled in ice, diluted with ethyl alcohol (35 ml), and sodium borohydride (0.743 g., 0.0196 mole) was added and the mixture was stirred overnight at 25° C. The solvent was removed under reduced pressure, the residue was dissolved in ethyl acetate, and the solution was washed with water and brine and then dried with sodium sulfate. The mixture was filtered, and the solvent removed under reduced pressure to give N-(3,5-difluoro-4-methoxybenzyl)-aminoacetaldehyde dimethyl acetal as an oil (4.94 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992459
Source datasetuspto-grants-1991_02
ORD IDord-a8a08d2d6cc84142aa32ff5792554b9f
Source noteuspto-grants-1991_02