Participants
| Role | Name | HCID | Charge |
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| Reactant | Urea | HCID 1176 | — |
| Reactant | HCID 57464352 | HCID 57464352 | — |
| Reactant | 5-(2-Methoxy-benzyl)-oxazol-2-ylamine | HCID 60027512 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Methoxyaniline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541453B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-b19003000c444e7a8d805808627dfd7d |
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| Source note | uspto-grants-2013_09 |
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