化工社化工社 化学情報印刷レポート · 研究参考用
m-(Trifluoromethyl)benzamide → 5-(alpha,alpha,alpha-Trifluoro-m-Tolyl)-1,3,4-Oxathiazol-2-One
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | m-(Trifluoromethyl)benzamide | HCID 74535 | — |
| 反応物 | (Chlorothio)formyl chloride | HCID 75990 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 5-(alpha,alpha,alpha-Trifluoro-m-Tolyl)-1,3,4-Oxathiazol-2-One | HCID 12260110 | 86.3% |
反応手順
α,α,α-Trifluoro-m-toluamide (82.7 g, 0.437 mol) and chlorocarbonylsulfenyl chloride (86 g, 0.667 mol, 53% excess) were reacted under the conditions of Example 2 for 0.5 hours. The light yellow residue was dissolved in ethyl acetate and cooled to -78°. The white precipitate was filtered and washed with hexane to yield 93.14 g (0.377 mol, 86.2%) of white solid, m.p. 85°-86.5°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04261728 |
| 出典データセット | uspto-grants-1981_04 |
| ORD ID | ord-745498c25ccc40d08310b90c6e84aa74 |
| 出典メモ | uspto-grants-1981_04 |