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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601621Generated: October 29, 2026

Formate → 2-(5-Ethyloxazol-2-yl)ethylamine

https://huagongshe.com/reaction/601621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormateHCID 283—
ReactantBenzyl [2-(5-ethyloxazol-2-yl)ethyl]carbamateHCID 57636953—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(5-Ethyloxazol-2-yl)ethylamineHCID 11542801—

Reaction Steps

Ammnonium 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 numberUS07902375B2
Source datasetuspto-grants-2011_03
ORD IDord-85fabe98a36d485ab1df99a083387309
Source noteuspto-grants-2011_03