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Water → 2-((2-Chloro-4-nitrophenoxy)methyl)thiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-Chloro-1-fluoro-4-nitrobenzene | HCID 67688 | — |
| 反応物 | 1,3-Thiazol-2-ylmethanol | HCID 2795213 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-((2-Chloro-4-nitrophenoxy)methyl)thiazole | HCID 53401006 | 99.2% |
反応手順
2-(2-Chloro-4-nitro-phenoxymethyl)-thiazole is prepared by adding thiazol-2-yl-methanol (2.74 g, 23.76 mmol) to a slurry of sodium hydride (1.21 g of a 60% dispersion in oil, 30.2 mmol) in DMF (10 ml) at 0° C. After several minutes, 2-chloro-1-fluoro-4-nitro-benzene (3.79 g, 21.60 mmol) is added and the reaction mixture warmed to room temperature. The reaction mixture is stirred at room temperature for 3 h, and 60° C. for 16 h. After cooling to room temperature, the reaction mixture is poured into 200 ml water. The resulting precipitate is collected by filtration, washed with water, and dried in vacuo to give 2-(2-chloro-4-nitrophenoxymethyl)-thiazole (5.80 g, 99%) which is used without further purification .
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07501427B2 |
| 出典データセット | uspto-grants-2009_03 |
| ORD ID | ord-985532295722483ba0fcf54e9aaada80 |
| 出典メモ | uspto-grants-2009_03 |