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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609285Generated: October 30, 2026

2-Aminothiophenol → 2-(2-Aminophenyl)sulfanylbenzonitrile

https://huagongshe.com/reaction/1609285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiophenolHCID 8713—
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChlorobenzonitrileHCID 13391—
SolventDimethylformamideHCID 6228—
Product2-(2-Aminophenyl)sulfanylbenzonitrileHCID 36623384.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

In 10 ml of DMF was dissolved 1.25 g of orthoaminothiophenol followed by addition of 1.38 g of potassium carbonate. The mixture was preheated at 100° C. and after 1.45 g of o-chlorobenzonitrile was added, the mixture was stirred in an argon gas stream at 100° C. for 1 hour. To the reaction mixture was added ice-water and the mixture was extracted with ethyl acetate. The extract was washed with water twice and dried over magnesium sulfate and the solvent was distilled off. The residue was crystallized from n-hexane-isopropyl ether to give 1.91 g of the title compound as white crystals, m.p. 88°-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399703
Source datasetuspto-grants-1995_03
ORD IDord-e4752e23f9ad422380fae808ae1345c7
Source noteuspto-grants-1995_03