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HRID 53702作成日:2026年10月24日

Stannous Chloride → 3-Chloro-4,5-difluoro-1,2-diaminobenzene

https://huagongshe.com/ja/reaction/53702

反応式

関与物質

役割名称HCID仕込み量
反応物Stannous ChlorideHCID 24479—
反応物Sodium BicarbonateHCID 516892—
反応物1,2-Diamino-4,5-difluorobenzeneHCID 2736755—
反応物2-Chloro-3,4-difluoro-6-nitroanilineHCID 14365248—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物3-Chloro-4,5-difluoro-1,2-diaminobenzeneHCID 19958589—

反応手順

3-Chloro-4,5-difluoro-1,2-diaminobenzene was prepared using an adaptation of the method of Bellamy et al. (Bellamy, F. D. et al., Tetrahedron Lett. 25: 839 (1984)) A mixture of 2-chloro-3,4-difluoro-6-nitroaniline (160 mg, 0.767 mmol) and SnCl2 2H2O (0.863 g, 3.84 mmol) was dissolved in 5 mL ethyl acetate and 2 mL absolute ethanol under N2 and heated at 75 ° C. for 5 h. The reaction was allowed to cool to room temperature and poured into 50 mL H2O. Sufficient sat'd NaHCO3 solution was added (foaming!) to bring the pH to 7. The resulting mixture was extracted with 3×20 mL ethyl acetate and the combined organic extracts washed with 20 mL sat'd NaCl solution. The organic phase was dried (MgSO4), vacuum filtered and the solvent rotary evaporated to yield a brown solid, 124 mg (91%). 1H NMR (CDCl3) δ 3.52 (br s, 4H, 2(NH2)); 6.49 (dd, 1H, JHF =7.5, 10.8 Hz, H-6). There was 13% 4,5-difluoro-1,2-diaminobenzene present by NMR.

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-f91013e2377d4a02a8e68411c32e3c4e
出典メモuspto-grants-1997_04