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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404714Generated: October 25, 2026

4-Bromobenzaldehyde → N-(4-Bromobenzyl)-2,2-dimethoxyethanamine

https://huagongshe.com/reaction/404714

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzaldehydeHCID 70741—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantSodium borohydrideHCID 4311764—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
ProductN-(4-Bromobenzyl)-2,2-dimethoxyethanamineHCID 5922624181.7%

Reaction Steps

50 g (270.2 mmol) 4-bromobenzaldehyde were dissolved in 200 ml of toluene and 28.4 g (270.2 mmol) aminoacetaldehyde dimethylacetal were added. After the addition of 5.1 g (27.0 mmol) p-toluenesulfonic acid monohydrate, the reaction mixture was heated under reflux in a Dean Stark apparatus. After 4 h, the reaction was cooled to room temperature and washed with saturated sodium hydrogen carbonate-solution (2×) and water. The combined aqueous layers were extracted with Toluene and the combined organic layers were dried over magnesium sulfate and evaporated. The residue was dissolved in 200 ml of ethanol and 5.11 g (135.1 mmol) of sodium borohydride were added in small portions. After stirring for 2 h at room temperature and standing overnight, 5.0 ml acetic acid were added and the solvent was removed i. vac. The residue was taken up in dichloromethane and washed (2×) with water. After drying over magnesium sulfate and evaporation, 60.5 g of the title compound were obtained (crude product), which were used without further purification. Rt=0.80 min (Method C). Detected mass: 274.1/276.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748614B2
Source datasetuspto-grants-2014_06
ORD IDord-5d4402caa3d54c78a237de7453d9ab3a
Source noteuspto-grants-2014_06