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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964796Generated: November 1, 2026

Ethanolamine → 2-[(2-Furylmethyl)amino]ethanol

https://huagongshe.com/reaction/1964796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantFurfuralHCID 7362—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantPeptide oostatic hormoneHCID 5488810—
Solvent1,2-DichloroethaneHCID 11—
Product2-[(2-Furylmethyl)amino]ethanolHCID 4722610—

Reaction Steps

An aldehyde, e.g., 2-furfuraldehyde (2 g, 20.82 mmol), and an amine, e.g., 2-aminoethanol, (1.65 g, 27.06 mmol) were poured together in a mixture 1:1 TMOF:DCE (50 ml) and the reaction mixture was cooled down to zero degree. The reducing agent NaBH(OAc)3 (6.18 g, 29.14 mmol) was added in 4 subsequent portions over a 5 min period, the reaction mixture was allowed to gradually warm to room temperature and stirred for 16 hours. The solvents was removed from the reaction in vacuo and the residue was partitioned between dichloromethane (150 ml) and saturated bicarbonate solution (50 ml). After separation, the organic layer was washed with saturated bicarbonate solution (50 ml) and brine (50 ml). The combined organic layers were then dried over sodium sulphate, filtered and the solvent removed in vacuo. The desired secondary amines, e.g., 2-[(2-furylmethyl)amino]ethanol, were obtained as a yellowish oil (1.82 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415480B2
Source datasetuspto-grants-2013_04
ORD IDord-9be17ea6be714fdbbf3333201b4abd9a
Source noteuspto-grants-2013_04