HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981570Generated: October 31, 2026
3-Fluoro-p-anisaldehyde → N-(2,2-Dimethoxyethyl)-3-fluoro-4-methoxybenzenemethanamine
https://huagongshe.com/reaction/981570
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluoro-p-anisaldehyde | HCID 67696 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(2,2-Dimethoxyethyl)-3-fluoro-4-methoxybenzenemethanamine | HCID 20070446 | 85% |
Reaction Steps
3--Fluoro-4-methoxybenzaldehyde (5.0 g, 0.0324 mole) was added to aminoacetaldehyde dimethyl acetal (3.53 ml, 0.0324 mole) and the mixture was heated at 100° C. for 2 hours. The reaction mixture was cooled in ice, diluted with ethyl alcohol (50 ml) and sodium borohydride (1.23 g, 0.0324 mole) was added and the mixture was stirred overnight at 25° C. The solvent was removed under reduced pressure and 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-fluoro-4-methoxybenzyl)-aminoacetaldehyde dimethyl acetal as an oil (6.68 g, 85%).
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-f948ea37d65c40ac9d274b94f93ce13a |
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| Source note | uspto-grants-1991_02 |
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