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4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedione → 2-(5-Furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-benzoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedione | HCID 67594 | — |
| 反応物 | 2-Hydrazinobenzoic acid | HCID 79223 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2-(5-Furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-benzoic acid | HCID 11415997 | — |
反応手順
4,4,4-Trifluoro-1-(2-furyl)-1,3-butanedione (2.4 mL, 16 mmol) was added to 2-hydrazinobenzoic acid (3.01 g, 16 mmol) in acetic acid (20 mL) and heated at reflux for 25 h. The reaction was cooled, diluted with EtOAc, and extracted twice with water. The organic layer was dried over Na2SO4, filtered, and evaporated to yield a thick red paste (5.71 g, >100%). 1H NMR (CDCl3) δ8.18 (dd, 1H, J=7.7, J′=1.8), 7.74 (td, 1H, J=7.7, J′=1.4), 7.65 (td, 1H, J=7.7, J′=1.5), 7.50 (dd, 1H, J=7.3, J′=1.1), 7.35 (m, 1H), 6.89 (s, 1H), 6.28 (m, 1H), 5.76 (d, 1H, J=3.3).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06271237B1 |
| 出典データセット | uspto-grants-2001_08 |
| ORD ID | ord-db6e33ec60db41e0b3064a86bc5b5335 |
| 出典メモ | uspto-grants-2001_08 |