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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407282Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/407282

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-4-fluoro-2-nitrobenzeneHCID 67659—
EduktSodium sulfide nonahydrateHCID 73972—
LösungsmittelWaterHCID 962—
Produkt2-Amino-4-fluorobenzene-1-thiolHCID 1110548025%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754233B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-022647257f5a424ca792ce8d58f398c5
Quellennotizuspto-grants-2014_06