Ethyl 2-(diethoxymethyl)thiazole-4-carboxylate → Ethyl 2-formyl-1,3-thiazole-4-carboxylate
反応式
C([O:3][CH:4](OCC)[C:5]1[S:6][CH:7]=[C:8]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[N:9]=1)C>Cl.CC(C)=O>[CH:4]([C:5]1[S:6][CH:7]=[C:8]([C:10]([O:12][CH2:13][CH3:14])=[O:11])[N:9]=1)=[O:3]参加物
4
実験手順
A solution of ethyl 2-[bis(ethyloxy)methyl]-1,3-thiazole-4-carboxylate (455 mg) in 10% 1M hydrochloric acid in acetone (50 ml) was heated at reflux for 1 h. The mixture was concentrated in vacuo, taken up in DCM (20 ml) and washed with saturated sodium bicarbonate solution (10 ml). The organic layer was separated using a hydrophobic frit and evaporated to give the title compound (317 mg) as a yellow solid.
後処理
- temperatureat reflux for 1 h
- concentrationThe mixture was concentrated in vacuo
- washwashed with saturated sodium bicarbonate solution (10 ml)
- customThe organic layer was separated
- customevaporated
出典と根拠
- ORDレコード
- ord-8b26753199ef4372a0c393a59c494455
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08658635B2
反応ノート
読み込み中…