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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398086Generated: October 27, 2026

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

https://huagongshe.com/reaction/398086

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 numberUS06610747B2
Source datasetuspto-grants-2003_08
ORD IDord-76eb74a912a34d528fe9645b42d50541
Source noteuspto-grants-2003_08