Acetic Anhydride → 5-(1'-Ethoxyethylidene)-3-ethylrhodanine
反応式
[CH2:1]([N:3]1[C:7](=[O:8])[CH2:6][S:5][C:4]1=[S:9])[CH3:2].C(C(CC)(CC)C([O-])([O-])[O-])C.[C:21]([O:24][C:25](=O)[CH3:26])(=O)[CH3:22]>>[CH2:21]([O:24][C:25](=[C:6]1[S:5][C:4](=[S:9])[N:3]([CH2:1][CH3:2])[C:7]1=[O:8])[CH3:26])[CH3:22]参加物
実験手順
A mixture of 5 g. (0.033 m.) of 3-ethylrhodanine, 12 ml. of triethylorthoacetate and 35 ml. of acetic anhydride is heated under reflux for 18 hours and the solution is then concentrated in vacuo. The cooled residue is filtered and the solid is dissolved in ether. The ether solution is washed with water, dried and evaporated in vacuo to give 5-(1'-ethoxyethylidene)-3-ethylrhodanine. The latter (3.6 g.) is stirred with 15 ml. of dioxane, 15 ml. of water and 15 ml. of 10% sodium hydroxide solution for 4 hours. The resulting solution is concentrated in vacuo at 40°C. and the aqueous solution is washed with ether, decolorized, then made acidic with dilute hydrochloric acid. The precipitate is dissolved in 10% sodium hydroxide solution, washed with ether and the aqueous solution is made acidic with dilute hydrochloric acid to give the product, 3-ethyl-5-(1'-hydroxyethylidene)-rhodanine, m.p. 93°C.
後処理
- additionA mixture of 5 g
- temperatureunder reflux for 18 hours
- concentrationthe solution is then concentrated in vacuo
- filtrationThe cooled residue is filtered
- dissolutionthe solid is dissolved in ether
- washThe ether solution is washed with water
- customdried
- customevaporated in vacuo
出典と根拠
- ORDレコード
- ord-17f3118bac2546dba5a7f6455b14fa4c
- 出典データセット
- uspto-grants-1976_06
- 特許番号
- US03966942
反応ノート
読み込み中…