戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 416614作成日:2026年10月25日

2-Bromo-2'-nitroacetophenone → 4-(2-Nitrophenyl)thiazole-2-amine

https://huagongshe.com/reaction/416614

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromo-2'-nitroacetophenoneHCID 244025—
反応物ThioureaHCID 2723790—
溶媒EthanolHCID 702—
生成物4-(2-Nitrophenyl)thiazole-2-amineHCID 595779—

反応手順

4-(2-Nitro-phenyl)-thiazol-2-ylamine was prepared as follows: 2-Bromo-2′-nitroacetophenone (1.75 g, 7.2 mmol) was mixed with 50 mL of absolute EtOH along with thiourea (1.09 g, 14.4 mmol) and stirred under reflux for 2 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting residue was basified with 20 mL of 1 N aqueous NaOH and extracted with CH2Cl2. The combined organic layers were dried (Na2SO4) and concentrated to afford essentially quantitative yield of 4-(2-nitro-phenyl)-thiazol-2-ylamine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088928B2
出典データセットuspto-grants-2012_01
ORD IDord-f45d86eaa3234b0bbb13b75f84f29e24
出典メモuspto-grants-2012_01