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HRID 53726作成日:2026年10月25日

Ethanol → 3-Bromo-5-fluorobenzene-1,2-diamine

https://huagongshe.com/reaction/53726

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Stannous ChlorideHCID 24479—
反応物2-Bromo-4-fluoro-6-nitroanilineHCID 292004—
反応物Sodium BicarbonateHCID 516892—
溶媒Ethyl AcetateHCID 8857—
生成物3-Bromo-5-fluorobenzene-1,2-diamineHCID 14029989—

反応手順

1,2-Diamino-3-bromo-5-fluorobenzene was prepared using an adaptation of the method of Bellamy et al., Tetrahedron Lett. 25: 839 (1984). A mixture of 6-bromo-4-fluoro-2-nitroaniline (673 mg, 2.87 mmol) and SnCl2 2H2O (3.23 g, 14.3 mmol) dissolved in 6 mL ethyl acetate and 3 mL absolute ethanol was heated at 70° C. for 30 min. All the starting material had reacted as evidenced by TLC (silica gel, 2:1 hexanes:ethyl acetate). The reaction was allowed to cool to room temperature and poured into 20 mL crushed ice. Sufficient solid NaHCO3 was added to bring the pH to 7.5. The reaction mixture was then extracted with 3×20 mL ethyl acetate and the combined organic phases washed with sat'd NaCl solution. The organic phase was dried (MgSO4), vacuum filtered and the solvent rotary evaporated to yield a dark brown liquid 510 mg (86.7%). 1H NMR (CDCl3) δ 3.64 (br s, 4H, 2(NH2)), 6.44 (dd, 1H, H5, J4-5 =2.7, JH-F =9.8), 6.72 (dd, 1H, H4, J4-5 =2.7, JHF =8.4).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05620979
出典データセットuspto-grants-1997_04
ORD IDord-95213e157b52418ab3bef0f7f515d672
出典メモuspto-grants-1997_04