戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1024428作成日:2026年10月25日

Water → Ethyl 5-(4-nitrophenyl)thiazole-2-carboxylate

https://huagongshe.com/reaction/1024428

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium CarbonateHCID 10340—
反応物Lawesson's reagentHCID 87949—
反応物Ethyl 2-(2-(4-nitrophenyl)-2-oxoethylamino)-2-oxoacetateHCID 66572182—
溶媒Ethyl AcetateHCID 8857—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl 5-(4-nitrophenyl)thiazole-2-carboxylateHCID 5340468273.5%

反応手順

A solution of Ethyl 2-(2-(4-nitrophenyl)-2-oxoethylamino)-2-oxoacetate (Intermediate 1, step C, 5 g) and Lawesson's reagent (7.22 g) in 1,4-Dioxane (100 ml) was refluxed for 2 hours. The reaction mixture was cooled, water was added and the mixture was neutralized with saturated solution of Na2CO3. This was followed by addition of EtOAc and then the layers were separated. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to get dark brown residue. The residue was chromatographed on silica gel in 0.5:9.5 EtOAc:CHCl3 to get dark yellow colored solid which was crystallized in CHCl3/pet ether to yield 3.65 g (73%) of the title compound. 1H NMR (CDCl3, 300 MHz): δ 8.33 (d, 2H), 8.3 (s, 1H), 7.83 (d, 2H), 4.54 (q, 2H), 1.49 (t, 3H); MS (ES+) m/z 279 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722901B2
出典データセットuspto-grants-2014_05
ORD IDord-768940d956a8419c9a984d241c5ef41d
出典メモuspto-grants-2014_05