HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506243Generated: October 31, 2026
3-Hydroxyanthranilic Acid → Methyl 2-(4-fluorophenyl)benzoxazole-4-carboxylate
https://huagongshe.com/reaction/506243
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Hydroxyanthranilic Acid | HCID 86 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(4-fluorophenyl)benzoxazole-4-carboxylate | HCID 59626027 | 26% |
| Product | 2-(4-Fluorophenyl)benzoxazole-4-carboxylic acid | HCID 59626030 | — |
Reaction Steps
2-(4-fluorophenyl)benzoxazole-4-carboxylic acid was prepared from 3-hydroxyanthranilic acid and 4-fluorobenzoyl chloride as described in Step A of Example 1. The crude product was dissolved in methylene chloride (20 mL) and the resulting solution treated with oxalyl chloride (1 mL) and DMF (0.05 mL). After stirring at room temperature for 6 h, the reaction was quenched by the addition of methanol (10 mL) and stirred at room temperature for a further 71 h. The reaction was then re-concentrated and the resulting solid purified by column chromatography to afford a 26% yield of methyl 2-(4-fluorophenyl)benzoxazole-4-carboxylate as a white solid: 1H NMR (500 MHz, CDCl3) δ 8.36 (dd, J=14.7, 11.8 Hz, 2H), 8.03 (d, J=14.7 Hz, 1H), 7.78 (d, J=15.2 Hz, 1H), 7.42 (t, J=13.2 Hz, 1H), 7.18 (m, 2H), 4.06 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781430B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-72214cb3875c45c395da1366f10bffc0 |
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| Source note | uspto-grants-2010_08 |
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