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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974809Generated: October 30, 2026

2-Aminothiophenol → HCID 19969463, compound

https://huagongshe.com/reaction/974809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantSodium hydrideHCID 24758—
Reactant2-Fluoro-5-nitrobenzonitrileHCID 519417—
SolventDimethylformamideHCID 6228—
ProductHCID 19969463HCID 19969463—

Reaction Steps

2-Aminothiophenol (6.26 g, 50 mmol) was added to a mixture of sodium hydride (2.0 g of 60% oil dispersion, 50 mmol) in DMF (100 ml) at 0° under nitrogen. After stirring for 30 minutes at 0°, 2-fluoro-5-nitrobenzonitrile (8.3 g, 50 mmol) in DMF (20 ml) was added and the mixture kept at room temperature overnight. The reaction mixture was evaporated and azeotroped with toluene, then the residue was partitioned between chloroform and water and the layers separated. Drying (sodium sulphate) and evaporation of the organic layer gave a residue which was separated from chloroform as bright yellow crystals (10.1 g, Rf 0.52 in 1:1 ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607929
Source datasetuspto-grants-1997_03
ORD IDord-261cc5b59d4b4cfcb1d41aa11b6cc69b
Source noteuspto-grants-1997_03