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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946837Generated: November 2, 2026

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

https://huagongshe.com/reaction/1946837

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): δ 8.77 (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 numberUS08399456B2
Source datasetuspto-grants-2013_03
ORD IDord-dcbba5cf002d405885597bb8fd737a07
Source noteuspto-grants-2013_03