化工社化工社 化学情報印刷レポート · 研究参考用
Chloroacetaldehyde → Thiazole, 2-[(3,4,4-trifluoro-3-butenyl)thio]-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Chloroacetaldehyde | HCID 33 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 3,4,4-Trifluoro-3-butenyl dithiocarbamate | HCID 11298598 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | Thiazole, 2-[(3,4,4-trifluoro-3-butenyl)thio]- | HCID 11447455 | — |
反応手順
15.1 g (64.8 mmol; purity 86.3%) of 3,4,4-trifluoro-3-butenyl dithiocarbamate in 100 ml of dioxane are admixed with 0.2 ml of conc. hydrochloric acid and 12.4 g (71.2 mmol) of 45% aqueous chloroacetaldehyde solution. The mixture is boiled for 4 h under argon, and another 1 ml of chloroacetaldehyde solution is added after 2 h. The mixture is then concentrated by evaporation under reduced pressure, the residue taken up in dichloromethane and washed with water, and the organic phase concentrated by evaporation under reduced pressure after drying over MgSO4. 16 g (94.4% of theory; purity by GC/MS: 86.1 area %) of an oil are obtained, which may be distilled at 0.4 T/86° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07439408B2 |
| 出典データセット | uspto-grants-2008_10 |
| ORD ID | ord-e494e05befe84184b27d75692c70f54b |
| 出典メモ | uspto-grants-2008_10 |