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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401594Generated: October 27, 2026

Urea → 5-Benzyloxazol-2-amine

https://huagongshe.com/reaction/401594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantBenzenepropanalHCID 7707—
Reactant2-Bromo-3-phenylpropanalHCID 11390228—
SolventEthanolHCID 702—
Product5-Benzyloxazol-2-amineHCID 60027526—

Reaction Steps

A mixture of 2-bromo-3-phenylpropionaldehyde (14.2 g, crude from above) and urea (7.2 g, 0.12 mol) were heated to reflux for 15 hours in 200 mL of ethanol. The solvent was evaporated to dryness and the residue was diluted with dichloromethane (250 mL) and then washed with sodium hydroxide (10% aqueous solution, 100 mL) and water (50 mL). The organic layer was extracted three times with hydrochloric acid (5% aqueous solution, 250 mL). The combined aqueous layers were adjusted to between pH 9 to 10 with a 10% aqueous solution of sodium hydroxide and then extracted three times with dichloromethane (300 mL). The organic layer was dried over sodium sulfate, evaporated to dryness, and purified by silica gel column chromatography to give a pale yellow solid. (1.6 g, 9.2 mmol, 9.2% from 3-phenyl-propionaldehyde). ESI-MS m/z calc. 174.1. found 175.1 1H NMR (CDCl3) δ 7.32-7.22 (m, 5H), 6.39 (s, 1H), 4.72 (bs, 2H), 3.84 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741939B2
Source datasetuspto-grants-2014_06
ORD IDord-a924fb029ac342f9b631ff12b9cb1182
Source noteuspto-grants-2014_06