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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426695Generated: November 4, 2026

Hydrochloric Acid → [(2,4-Dimethoxyphenyl)methyl](methyl)amine

https://huagongshe.com/reaction/1426695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylamineHCID 6329—
Reactant2,4-DimethoxybenzaldehydeHCID 69175—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product[(2,4-Dimethoxyphenyl)methyl](methyl)amineHCID 241653681%

Reaction Steps

2,4-Dimethoxybenzaldehyde (5.0 g) was dissolved in methanol (60 mL), and a 40% methanol solution (9.3 mL) of methylamine was added at room temperature. The mixture was stirred at room temperature for 1 hr, and sodium borohydride (1.37 g) was added by small portions under ice-cooling. The mixture was stirred at room temperature for 3 hr, treated with 1 mol/L hydrochloric acid under ice-cooling, and methanol was evaporated under reduced pressure. The residue was diluted with ethyl acetate, basified with saturated aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent: hexane:ethyl acetate=4:1→2:1) to give the title compound as a colorless oil (yield 4.41 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-ebcde0bc413b4de382768e90dc2c129d
Source noteuspto-grants-2015_01