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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408588Generated: October 25, 2026

Ethanolamine → 2-(4-Chloro-benzylamino)-ethanol

https://huagongshe.com/reaction/408588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Chloro-benzylamino)-ethanolHCID 424452—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethanolamine (1.2 eq.) in either MeOH or THF were added NaHCO3 (1.5 eq.) and 4-chlorobenzaldehyde (1 eq.). The reaction was refluxed for 4 h, then cooled to 0° C. NaBH4 (1.2 eq.) was added portionwise. The reaction was stirred for 1 h at 0° C., then 15 h at 20° C. The crude was concentrated under reduced pressure then partitioned between water and DCM. The aqueous layer was then extracted twice with DCM. The organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with DCM/MeOH: 1/0 to 95/5) to afford 2-(4-chloro-benzylamino)-ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759334B2
Source datasetuspto-grants-2014_06
ORD IDord-bc4addb90c7f49ce91f792e1b8b06d90
Source noteuspto-grants-2014_06