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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327162Generated: October 29, 2026

Thiophenol → HCID 706762, compound

https://huagongshe.com/reaction/327162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Chloro-5-nitrobenzonitrileHCID 85504—
Reactant3111-52-2HCID 68683554—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 706762HCID 706762—

Reaction Conditions

Temperature105 °C

Reaction Steps

4-Chloro-3-cyanonitrobenzene (12.5 g, 6.84 mmol) was added portionwise to a stirred N,N-dimethylformamide (50 mL) solution of thiophenol potassium salt [prepared by adding thiophenol (7.1 mL, 6.9 mmol) to a solution of potassium hydroxide (3.84 g, 6.84 mmol) in methanol followed by removal of the methanol in vacuo]. After stirring at 105° C. for 2.5 hours the mixture was poured into ice-water, filtered, the collected solid washed with water, dissolved in 300 mL of refluxing ethanol (charcoal), filtered, treated with 35 mL of water and refrigerated. The resulting pale yellow solid weighed 13.3 g (76%), mp 82°-84° C. 1H--NMR (250 MHz, CDCl3): 6.93 (d, 1H, J=9.0 Hz, aromatic), 7.51-7.62 (m, 5H, aromatic), 8.12(dd, 1H, J=9.2, 2.5 Hz, aromatic), 8.46 (d, 1H, J=2.5 Hz, aromatic). MS (CI, CH4): 257(M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272163
Source datasetuspto-grants-1993_12
ORD IDord-598b0445225149e5a83d2c7ae88ca28e
Source noteuspto-grants-1993_12