Water → 2-Chloro-4-phenylthiazole-5-carboxylic acid
反応式
[Cl:1][C:2]1[S:3][C:4]([C:13]([O:15]CC)=[O:14])=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1.[OH-].[Na+].O>O1CCCC1>[Cl:1][C:2]1[S:3][C:4]([C:13]([OH:15])=[O:14])=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1参加物
5
実験手順
A mixture of 53.4 g (0.2 mole) of ethyl 2-chloro-4-phenyl-5-thiazolecarboxylate, 8.0 g (0.2 mole) of NaOH, 200 ml. of water and 400 ml. of tetrahydrofuran was stirred for 16 hours and extracted with ether. The organic layer was discarded. The aqueous layer was made acidic and the precipitate was collected and air-dried to give 43.2 g (90%) of the desired product, m.p. 170°-171° C.
後処理
- extractionextracted with ether
- customthe precipitate was collected
- customair-dried
出典と根拠
- ORDレコード
- ord-037f94191c814069bad2c02e159ffa2a
- 出典データセット
- uspto-grants-1982_06
- 特許番号
- US04336389
反応ノート
読み込み中…