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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzonitrile, 4-chloro-3-nitro- | HCID 13655 | — |
| Reactant | 2,5-Xylenethiol | HCID 77615 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2,5-Dimethylphenylthio)-3-nitrobenzonitrile | HCID 29106746 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399456B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-dcbba5cf002d405885597bb8fd737a07 |
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| Source note | uspto-grants-2013_03 |
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