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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951215Generated: November 4, 2026

Ammonium formate → 2-(5-Ethyloxazol-2-yl)ethylamine

https://huagongshe.com/reaction/1951215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantBenzyl [2-(5-ethyloxazol-2-yl)ethyl]carbamateHCID 57636953—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(5-Ethyloxazol-2-yl)ethylamineHCID 11542801—

Reaction Steps

Ammonium formate (0.316 g, 5 mmol) is added to a solution of [2-(5-ethyl-oxazol-2-yl)-ethyl]-carbamic acid benzyl ester (step 3) (1.66 mmol) in methanol (15 ml) and 10% Pd on carbon (125 mg) is added under an inert atmosphere. The mixture is stirred at ambient temperature for 2 hours. The catalyst is removed by filtration and the filtrate is evaporated. The residue is diluted with dichloromethane, filtered to remove undissolved solid and the solvent is removed. The residue is dissolved in DCM and treated with 1M aqueous sodium hydroxide solution (5 ml). The organic extract is separated, dried (MgSO4), filtered and the solvent is removed. Crystallisation from ethyl acetate/dichloromethane affords the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404684B2
Source datasetuspto-grants-2013_03
ORD IDord-8c57c747ab7541d1a5298eb3532375b0
Source noteuspto-grants-2013_03