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Dimethylformamide → 4-Chloro-2-ethylsulfanylbenzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Ethanethiol | HCID 6343 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-Chloro-2-fluorobenzaldehyde | HCID 2724908 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-Chloro-2-ethylsulfanylbenzaldehyde | HCID 114863540 | — |
反応手順
A mixture of 4.0 g of 4-chloro-2-fluorobenzaldehyde, 2.05 ml of ethanethiol, 3.82 g of potassium carbonate and 6 ml of DMF was stirred at room temperature for 6 hours, and was allowed to stand overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, then dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 3.57 g of 4-chloro-2-ethylsulfanylbenzaldehyde. 4-Chloro-2-ethylsulfanylbenzaldehyde
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09260436B2 |
| 出典データセット | uspto-grants-2016_02 |
| ORD ID | ord-da831eea23c848ef89f1c7d1f684dc92 |
| 出典メモ | uspto-grants-2016_02 |