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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3,5-Difluoro-4-methoxybenzaldehyde | HCID 14450860 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(3,5-difluoro-4-methoxybenzyl)-aminoacetaldehyde dimethyl acetal | HCID 14450862 | 96.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04992459 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-a8a08d2d6cc84142aa32ff5792554b9f |
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| Source note | uspto-grants-1991_02 |
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