Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544517Generated: October 26, 2026

N-Methylbenzylamine → 2-(N-benzyl-N-methylamino)-1-(2-furyl)ethanol

https://huagongshe.com/reaction/544517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylbenzylamineHCID 7669—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-1-(furan-2-yl)ethan-1-oneHCID 2795076—
SolventMethanolHCID 887—
Product2-(N-benzyl-N-methylamino)-1-(2-furyl)ethanolHCID 1331725168.8%

Reaction Steps

2-(Bromoacetyl)furan (95 g) is added slowly to a stirred mixture of 75 g of N-methylbenzylamine and 70 g of potassium carbonate in 300 ml of methanol at 20°-30° C. The mixture is stirred at room temperature for 2.5 hours, and the insoluble matter is filtered off. To the filtrate is added 20 g of sodium borohydride at 10°-20° C. with stirring, and the mixture is stirred at room temperature for 3 hours. The solvent is then distilled off under reduced pressure, water is added to the residue, and the separated oil is extracted with ethyl acetate. The extract is washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Distillation of the residue gives 80 g of 2-(N-benzyl-N-methylamino)-1-(2-furyl)ethanol as pale yellow viscous oil, boiling at 130°-138° C. (0.2 mmHg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04450165
Source datasetuspto-grants-1984_05
ORD IDord-6f9134d21a2f493cae0b3a9f72c341c1
Source noteuspto-grants-1984_05