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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804708Generated: October 30, 2026

2-(Methylamino)ethanol → 2-((4-Methoxy-3-nitrobenzyl)(methyl)amino)ethanol

https://huagongshe.com/reaction/1804708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylamino)ethanolHCID 8016—
ReactantTriethylamineHCID 8471—
Reactant4-(Bromomethyl)-1-methoxy-2-nitrobenzeneHCID 11579648—
SolventAcetonitrileHCID 6342—
Product2-((4-Methoxy-3-nitrobenzyl)(methyl)amino)ethanolHCID 60968201—

Reaction Steps

A 5 mL round bottom flask was charged with 4-(bromomethyl)-1-methoxy-2-nitrobenzene (0.6 g, 2.44 mmol) and acetonitrile (2 mL). The solution was treated with triethylamine (1 mL, 7.32 mmol) and 2-(methylamino)ethanol (0.585 mL, 7.32 mmol) and the reaction was stirred at ambient temperature for 16 hours. The reaction was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated to provide the title compound. MS (DCI(+)) m/e 241.1 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354422B2
Source datasetuspto-grants-2013_01
ORD IDord-8fc888170e094715ae3136b3d5bc0bb4
Source noteuspto-grants-2013_01