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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407282Generated: October 26, 2026

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

https://huagongshe.com/reaction/407282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-fluoro-2-nitrobenzeneHCID 67659—
ReactantSodium sulfide nonahydrateHCID 73972—
SolventWaterHCID 962—
Product2-Amino-4-fluorobenzene-1-thiolHCID 1110548025%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754233B2
Source datasetuspto-grants-2014_06
ORD IDord-022647257f5a424ca792ce8d58f398c5
Source noteuspto-grants-2014_06