化工社化工社 化学情報印刷レポート · 研究参考用
p-Toluenesulfonic acid → 1,3-Dithiane-2-carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 1,3-Propanedithiol | HCID 8013 | — |
| 反応物 | Glyoxylic acid, monohydrate | HCID 15620607 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 1,3-Dithiane-2-carboxylic acid | HCID 303705 | — |
反応手順
9.20 g (100 mmol) of glyoxalic acid monohydrate, 11.1 ml (110 mmol) of 1,3-propanedithiol and 1.72 g (10.0 mmol) of para-toluenesulphonic acid were heated in 200 ml of toluene under reflux for 3 h. The reaction mixture was cooled to RT and extracted three times with 100 ml of saturated aqueous sodium bicarbonate solution. The combined aqueous phases were washed with 200 ml of diethyl ether, acidified with aqueous hydrochloric acid (6N) and extracted four times with 200 ml of ethyl acetate. The combined organic phases were dried over magnesium sulphate and filtered, and the solvent was removed under reduced pressure. The residue was used for the next step without further purification. Yield: 8.0 g (47% of theory)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09434690B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-44198022921e4074961d14a1761bdab7 |
| 出典メモ | uspto-grants-2016_09 |