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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184369Generated: November 2, 2026

Ethyl Acetate → 4-(2,5-Dimethylphenylthio)-3-nitrobenzonitrile

https://huagongshe.com/reaction/1184369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzonitrile, 4-chloro-3-nitro-HCID 13655—
Reactant2,5-XylenethiolHCID 77615—
SolventTetrahydrofuranHCID 8028—
Product4-(2,5-Dimethylphenylthio)-3-nitrobenzonitrileHCID 2910674695%

Reaction Steps

To a solution of 4-chloro-3-nitrobenzonitrile (5.4 g, 29.67 mmol) in THF (100 mL) was added 2,5-dimethylthiophenol (4.921 g, 35.60 mmol) and K2CO3 (20.45 g, 148.0 mmol). The reaction was monitored with TLC (25% EtOAc in hexanes). After refluxing for 16 hrs, the reaction was complete. The solid was filtered and washed with copious amounts of EtOAc. The filtrate was washed sequentially with saturated NaHCO3, water, saturated NaCl solution, dried over MgSO4, filtered, and evaporated in vacuo. The resulting solid was then sonicated in hexanes and filtered to yield compound 24 as a yellow/white solid (8.00 g, 97.8% HPLC purity, 95% yield). 1H NMR (500 MHz, DMSO-d6): δ8.77 (d, J=2 Hz, 1H), 7.94 (dd, J1=2 Hz, J2=8 Hz, 1H), 7.46 (s, 1H), 7.41 (d, J=8 Hz, 1H), 7.36 (d, J=8 Hz, 1H), 6.76 (d, J=8 Hz, 1H), 2.32 (s, 3H), 2.23 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669247B2
Source datasetuspto-grants-2014_03
ORD IDord-81b46ca2ce3e4ba49ac5258696959a7d
Source noteuspto-grants-2014_03