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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407282생성일: 2026년 10월 26일

1-Chloro-4-fluoro-2-nitrobenzene → 2-Amino-4-fluorobenzene-1-thiol

https://huagongshe.com/reaction/407282

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-4-fluoro-2-nitrobenzeneHCID 67659—
반응물Sodium sulfide nonahydrateHCID 73972—
용매WaterHCID 962—
생성물2-Amino-4-fluorobenzene-1-thiolHCID 1110548025%

반응 단계

To a solution of 2-chloro-5-fluoronitrobenzene (1.81 g, 10.31 mmol) dissolved in 30 mL of deionized water at room temperature was added sodium sulfide nonahydrate (9.90 g, 41.24 mmol) in a single portion. The resulting solution was heated to reflux and stirred under nitrogen for 32 hours. The resulting light yellow solution was then cooled to room temperature and was washed with 5×50 mL of ethyl acetate. The organic phase was dried over anhydrous magnesium sulfate, filtered, and evaporated to yield a yellow oil. The crude material was purified by flash chromatography eluting with CH2Cl2:MeOH=10:1 to yield 0.36 g (25%) of the title compound. MS (m/z, ES+): 144.0 (M+1, 100%); IR (KBr): 3430, 3340, 1615, 1573, 1482, 1281, 1248, 1172, 1124, 1044, 975, 840, 792 cm−1; 1H NMR (300 MHz, ppm, DMSO-d6) δ: 6.89 (dt, 1H), 6.50 (dd, 1H), 6.21 (dt, 1H), 5.80 (br s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754233B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-022647257f5a424ca792ce8d58f398c5
출처 메모uspto-grants-2014_06