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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45271Generated: October 28, 2026

Urea → 2-Methoxyaniline

https://huagongshe.com/reaction/45271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantHCID 57464352HCID 57464352—
Reactant5-(2-Methoxy-benzyl)-oxazol-2-ylamineHCID 60027512—
SolventEthanolHCID 702—
Product2-MethoxyanilineHCID 7000—

Reaction Steps

5-(2-Methoxy-benzyl)-oxazol-2-ylamine A mixture of 2-chloro-3-(2-methoxylphenyl)-propionaldehyde (10 g, crude from above) and urea (9.6 g, 0.16 mol) was dissolved in ethanol (250 mL) and then heated at reflux overnight. The solvent was evaporated to dryness. 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 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 separated, dried over sodium sulfate, and evaporated to dryness. The crude product was purified by silica gel column chromatography to yield the yellow-red solid product (0.72 g, 0.35% from 2-methoxyaniline). ESI-MS m/z calc. 204.1. found 205.1 (M+1)+; 1H NMR (CDCl3) δ 7.26-7.20 (m, 1H), 7.14 (d, J=7.2 Hz, 1H), 6.91-6.86 (m, 2H), 6.35 (s, 1H), 4.49 (bs, 2H), 3.85 (s, 2H), 3.82 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541453B2
Source datasetuspto-grants-2013_09
ORD IDord-b19003000c444e7a8d805808627dfd7d
Source noteuspto-grants-2013_09