関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl chloroformate | HCID 6586 | — |
| 反応物 | 4-Methylmorpholine | HCID 7972 | — |
| 反応物 | 2-[(3,4-Difluorophenyl)formamido]acetic acid | HCID 705141 | — |
| 反応物 | Carbonochloridate | HCID 21226386 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(3,4-difluorophenyl)oxazol-5(4H)-one | HCID 58054172 | 95% |
反応手順
To a solution of 2-(3,4-difluorobenzamido)acetic acid (5.18 g, 24.1 mmol) in THF (25 mL) in a 100 mL round-bottomed flask was added 4-methylmorpholine (2.44 g, 24.1 mmol) to give a colorless solution. The solution was cooled to −10° C. and methyl chloroformate (2.28 g, 24.1 mmol) was added slowly over the course of thirty minutes while maintaining the solution at −10° C. A white precipitate started to form almost immediately and the solution became increasingly orange in color. Once the addition of chloroformate was complete the solution was stirred at −10° C. for 1 hour and warmed to room temperature over the course of an hour. The solution was filtered through a glass frit and the remaining solid was washed thoroughly with THF until colorless. The combined filtrate was evaporated under reduced pressure to provide 2-(3,4-difluoro-phenyl)oxazol-5(4H)-one as a light orange solid (4.5 g, 95%). LCMS (+ESI) m/z 198.2 [M+H]+. 1H-NMR (CDCl3) δ 7.85 (m, 1H), 7.78 (m, 1H), 7.30 (m, 1H), 4.45 (s, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08835422B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-3ff912b6b45f4b76adbc9416e0211ae8 |
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| 出典メモ | uspto-grants-2014_09 |
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