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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325053Generated: October 30, 2026

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

https://huagongshe.com/reaction/325053

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 numberUS06221898B1
Source datasetuspto-grants-2001_04
ORD IDord-33ffd13a03974ccc9cd55a3d7d722357
Source noteuspto-grants-2001_04