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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791874Generated: November 3, 2026

2-Aminothiophenol → Amino-2-[2-(4-cyanophenyl)ethylthio]benzene

https://huagongshe.com/reaction/1791874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22033501HCID 22033501—
SolventEthanolHCID 702—
ProductAmino-2-[2-(4-cyanophenyl)ethylthio]benzeneHCID 2203354782.4%

Reaction Steps

4-Toluenesulfonic acid, 2-(4-cyanophenyl)ethyl ester (1.9 g; 6.3 mmol; from Example 18(i) above) and K2CO3 (2.0 g) were added to a solution of 2-aminothiophenol (0.875 g; 7.0 mmol) in EtOH (20 mL). The mixture was heated to reflux for 48 hours, cooled, filtered and concentrated in vacuo to an oil which was dissolved in EtOAc (50 mL) and washed with water (25 mL). The organic portion was dried (MgSO4) and concentrated. The residue was purified by flash chromatography (SiO2; Et2O:hexane (1:1)) to obtain 1.32 g (78%) of the sub-title product as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074820B2
Source datasetuspto-grants-2006_07
ORD IDord-aca5d9a5cf0247d095e0826dbde90a3e
Source noteuspto-grants-2006_07