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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792745Generated: November 3, 2026

1-Chloro-4-nitrobenzene → HCID 12692632, compound

https://huagongshe.com/reaction/1792745

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-nitrobenzeneHCID 7474—
Reactant4-MethoxybenzenethiolHCID 12765—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductHCID 12692632HCID 1269263296.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a suspension of NaH (4.2 g) in 100 mL of dry DMF under nitrogen was slowly added 14.02 g of 4-methoxythiophenol. The reaction mix was stirred until no further gas evolution occurred (circa 20 minutes). To this solution was added 15.76 g of 4-chloronitrobenzene dissolved in 100 ml of dry DMF, after which the mixture was heated to 120° C. for one hour. The reaction mix became red in colour during this time. The mixture was then cooled to room temperature and poured over 1000 g of crushed ice. The resulting yellow solid was filtered, washed several times with water, and dried to afford 25.29 g (96%) of 4-(4-methoxy-phenylsulfanyl)-nitrobenzene as a yellow solid. MS M+H; 264.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078401B2
Source datasetuspto-grants-2006_07
ORD IDord-e8d135ce721f44c28b38da57cc1c2746
Source noteuspto-grants-2006_07