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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54308생성일: 2026년 10월 24일

4,5-Difluoro-2-nitroaniline → 1,2-Diamino-4,5-difluorobenzene

https://huagongshe.com/ko/reaction/54308

반응식

참여 물질

역할이름HCID투입량
반응물4,5-Difluoro-2-nitroanilineHCID 157151—
반응물4-Fluorobenzene-1,2-diamineHCID 164584—
반응물Calcium ChlorideHCID 5284359—
촉매ZincHCID 23994—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물1,2-Diamino-4,5-difluorobenzeneHCID 2736755—

반응 단계

4,5-Difluoro-1,2-diaminobenzene was prepared using an adaptation of the method of Tsuji et al., (Tsuji, Y. et al., J. Org. Chem. 55:580 (1990)). Zn powder (942 mg, 14.4 mmol), CaCl2 (94.4 mg), H2O (1.0 mL) and 4.0 mL EtOH were combined and brought to reflux as described for 4-fluoro-1,2-diaminobenzene (see Example 11) and to this mixture was added slowly dropwise a solution of 4,5-difluoro-2-nitroaniline (200 mg, 1.15 mmol) in 2 mL EtOH. Analysis and workup were as described for 4-fluoro-1,2-diaminobenzene (Example 11) except that the reaction was dissolved in 5 mL H2O and the solution extracted with 3×10 mL Et2O. The organic layers were combined and treated with activated charcoal, dried (MgSO4) and filtered through a pad of Celite. The solvent was evaporated at reduced pressure to yield 111.5 mg (67.3%) of a brown crystalline solid. 1H NMR (CDCl3) δ3.34 (br s, 4H, NH2), 6.53 (t, 2H, ArH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622952
출처 데이터셋uspto-grants-1997_04
ORD IDord-cedfbb40da604e36b7e49d168acf96bb
출처 메모uspto-grants-1997_04