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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-p-anisaldehydeHCID 67696—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductN-(2,2-Dimethoxyethyl)-3-fluoro-4-methoxybenzenemethanamineHCID 2007044685%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992459
Source datasetuspto-grants-1991_02
ORD IDord-f948ea37d65c40ac9d274b94f93ce13a
Source noteuspto-grants-1991_02