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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246618Generated: October 27, 2026

2-Chloro-1-fluoro-4-nitrobenzene → 2-Chloro-1-(methylsulfanyl)-4-nitrobenzene

https://huagongshe.com/reaction/1246618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
ReactantSodium methanethiolateHCID 4378561—
CatalystSantonoxHCID 7308—
SolventDimethylformamideHCID 6228—
Product2-Chloro-1-(methylsulfanyl)-4-nitrobenzeneHCID 1056009452.3%

Reaction Steps

To a solution of 4-fluoro-3-chloronitrobenzene (27 g, 156 mmol) in DMF (150 mL) at room temperature was added 5-tert-butyl-4-hydroxy-2-methylphenyl sulfide (100 mg) followed by sodium thiomethoxide (NaSMe) (10 g, 143 mmol) and the reaction was stirred for 6 h. The DMF was removed in vacuo and the residue was partitioned between ether (1 L) and water (1 L). The ether layer was washed with water (1 L) and brine (1 L), dried (MgSO4) and the solvent was removed under reduced pressure. The residue was purified by column chromatography (SiO2; DCM: pentane 1:5 increasing polarity to 3:7) to give the title compound (15.22 g, 49%) as a yellow solid; δH (400 MHz, CDCl3) 2.53 (3H, s), 7.20 (1H, d), 8.09 (1H, dd), 8.20 (1H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129234B2
Source datasetuspto-grants-2006_10
ORD IDord-a95ffb8ff0b54e9396eea89f92132f68
Source noteuspto-grants-2006_10