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HRID 1938141作成日:2026年10月27日

Sodium Chloride → 2-(3-Chloro-phenoxy)-thiazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1938141

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物3-ChlorophenolHCID 7933—
反応物Ethyl 2-bromo-1,3-thiazole-4-carboxylateHCID 353965—
反応物Sodium MethoxideHCID 10942334—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物2-(3-Chloro-phenoxy)-thiazole-4-carboxylic acid ethyl esterHCID 2146860196.1%

反応手順

13.72 g (106.72 mmol) 3-chlorophenol were added to a mixture of 19.21 g (106.72 mmol) sodium methylate-solution (30% in methanol) and 200 ml toluene and the mixture stirred 15 minutes at room temperature. The solution was evaporated to dryness, the residue suspended in 100 ml of toluene and evaporated to dryness again. The residue was dissolved in 100 ml dimethylsulphoxide and 24 g (101.65 mmol) of ethyl-2-bromothiazole-4-carboxylate [prepared as in Example 1b] were added in one portion. The solution was stirred for 24 hours at 80° C., cooled to room temperature and poured into 1200 ml water. 200 ml of saturated sodium chloride solution were added and the mixture extracted three times with 300 ml toluene. The organic layers were combined and washed with 200 ml 0.1 m NaOH and 200 ml of diluted sodium chloride solution, dried over Na2SO4 and evaporated to dryness to give 27.72 g (96%) of pale brown oily ethyl-2-(3-chlorophenoxy)thiazole-4-carboxylate. NMR (CDCl3):1.35(t,3H,CH3); 4.4(q,2H,CH2); 7.3(m,4H,Arom.) 7.7(s,1H,arom.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05693594
出典データセットuspto-grants-1997_12
ORD IDord-a56cf3d2262f4455a713c14b4ca0f5b8
出典メモuspto-grants-1997_12