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HRID 407282作成日:2026年10月27日

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

https://huagongshe.com/reaction/407282

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-4-fluoro-2-nitrobenzeneHCID 67659—
反応物Sodium sulfide nonahydrateHCID 73972—
溶媒WaterHCID 962—
生成物2-Amino-4-fluorobenzene-1-thiolHCID 1110548025%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754233B2
出典データセットuspto-grants-2014_06
ORD IDord-022647257f5a424ca792ce8d58f398c5
出典メモuspto-grants-2014_06