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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548611Generated: October 30, 2026

Ethanolamine → 2-[(4-Methoxybenzyl)amino]ethanol

https://huagongshe.com/reaction/548611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantMethanolHCID 887—
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
Product2-[(4-Methoxybenzyl)amino]ethanolHCID 104469—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 1 L round bottom flask is charged with 2-aminoethanol (29 g, 213 mmol), 4-methoxybenzaldehyde (39 g, 639 mmol), methanol (250 mL) and acetic acid (75 mL) under a nitrogen atmosphere. The contents were cooled to 0° C. and sodium triacetoxyborohydride (50 g, 234 mmol) was added over a 20 minute period. The reaction mixture was stirred at room temperature for 18 hours, concentrated under reduced pressure and partitioned between water (500 mL) and ethyl acetate (500 mL). The ethyl acetate layer was washed with 3N HCl (400 mL). The HCl layer is separated, cooled to 0° C., made basic using 6N NaOH and extracted with dichloromethane (2×100 mL). The dichloromethane layer was dried over sodium sulfate and concentrated under reduced pressure to yield the title compound a as an oil (20 g). 1H-NMR of the oil was consistent with the desired structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943617B2
Source datasetuspto-grants-2011_05
ORD IDord-7a31ab6623104d0e8851f93e9c4dfdd3
Source noteuspto-grants-2011_05