戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 7769作成日:2026年10月23日

4-Bromo-2-nitrophenol → 2-Amino-4-Bromophenol

https://huagongshe.com/ja/reaction/7769

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromo-2-nitrophenolHCID 24364—
反応物Stannous chloride dihydrateHCID 61436—
反応物Sodium BicarbonateHCID 516892—
溶媒MethanolHCID 887—
生成物2-Amino-4-BromophenolHCID 351840—

反応手順

To a stirred solution of 4-bromo-2-nitrophenol (5.00 g, 22.9 mmol) in MeOH (120 mL) was added tin(II) chloride dihydrate (15.53 g, 68.8 mmol). The reaction mixture was heated at reflux and monitored by LC/MS. When significant reduction was complete, the reaction mixture was cooled to rt, poured over ice, and made basic (pH 9) with 50% saturated NaHCO3. The aqueous layer was extracted with EtOAc (2×150 mL) and the combined extracts washed with brine, dried over MgSO4, filtered, and concentrated in vacuo to give 2-amino-4-bromophenol as a dark gray solid. 1H NMR (CDCl3, 300 MHz) δ 9.29 (br s, 1H), 6.71 (d, 1H), 6.56 (d, 1H), 6.49 (dd, 1H), 4.83 (br s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087601B2
出典データセットuspto-grants-2006_08
ORD IDord-c8eb1ab15de24a91a8d47e2209a31578
出典メモuspto-grants-2006_08