反応式
Cl.[CH2:2]([C:5]1[S:6][C:7]([C:10]([OH:12])=[O:11])=[CH:8][N:9]=1)[CH2:3][CH3:4].[CH2:13](O)[CH3:14]>>[CH2:2]([C:5]1[S:6][C:7]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:8][N:9]=1)[CH2:3][CH3:4]参加物
4
実験手順
A current of hydrochloric acid gas was passed with stirring through a solution of 30 g of 2-propyl-thiazole-5-carboxylic acid in 400 ml of absolute ethanol overnight and the ethanol was then evaporated off. The oily residue was taken up in ether containing 10% of potassium carbonate and the mixture was extracted with ether. The ether extracts were washed with water until a pH of 6 was obtained and the resulting yellow oil was purified by distillation to obtain 31.2 g of ethyl 2-propyl-thiazole-5-carboxylate with a boiling point of 139°-140° C. at 16 mmHg.
後処理
- customthe ethanol was then evaporated off
- extractionthe mixture was extracted with ether
- washThe ether extracts were washed with water until a pH of 6
- customwas obtained
- distillationthe resulting yellow oil was purified by distillation
出典と根拠
- ORDレコード
- ord-c55c881f656747d88e98efbd51af80b0
- 出典データセット
- uspto-grants-1977_09
- 特許番号
- US04046902
関連ノート
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