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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301600Generated: October 31, 2026

Ethanolamine → 2-(Benzyloxy)ethanamine

https://huagongshe.com/reaction/2301600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzyloxy)ethanamineHCID 53386890.8%

Reaction Steps

To a solution of ethanolamine (5 g, 81.8 mmol) in 100 mL of dried THF was added 60% NaH (3.27 g, 81.8mmol) at room temperature. The mixture was heated to reflux for 30min, then benzyl chloride (9.32 g, 73.6 mmol) was added. The resulting mixture was refluxed for 3 hours. The mixture was concentrated, the residue was diluted with 1 N aq. HCl, extracted with dichloromethane. The aqueous layer was adjusted to pH>14 with 10% aq. NaOH, extracted with dichloromethane. The organic was dried over MgSO4, concentrated to give desired product (10.11 g, 82%). 1H NMR (CDCl3): δ 7.34 (m, 5H), 4.54 (s, 2H), 3.54 (t, 2H), 2.93 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500863B1
Source datasetuspto-grants-2002_12
ORD IDord-72475dc8810c4bd69388317a5a8f84c0
Source noteuspto-grants-2002_12