HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660032Generated: October 26, 2026
Trifluoroacetic acid → 4-Cyano-2-isobutylpyridine
https://huagongshe.com/reaction/660032
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-Cyanopyridine | HCID 7506 | — |
| Reactant | Isovaleric Acid | HCID 10430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Chlorobenzene water | HCID 19815812 | — |
| Product | 4-Cyano-2-isobutylpyridine | HCID 14641786 | 54% |
Reaction Steps
p-cyanopyridine (8.00 g, 76.8 mmol) was added to a 1:1 mixture of chlorobenzene/water (1.5 L) in a 2 L round-bottom flask. Isovaleric acid (21.74 g, 212.8 mmol), (NH4)2S2O8 (34.40 g, 150.7 mmol), trifluoroacetic acid (8.78 g, 77.0 mmol) and AgNO3 (1.040 g, 6.1 mmol) were added and the heterogeneous mixture was vigorously stirred and refluxed for 2 h. The reaction was cooled down to 0° C. and 8 M NaOH was added slowly until pH 9-10. The mixture was filtered through Celite and extracted with EtOAc (×3). The combined organic extracts were dried with MgSO4 and the solvent removed in vacuo. The dark-brown oil was purified via flash chromatography (1:4 EtOAc/Hexane) to give a brown oil (6.538 g, 54%);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084471B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-1bc1b13d81f64304970f530af7fa27c3 |
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| Source note | uspto-grants-2011_12 |
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