HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660033Generated: October 26, 2026
Phenylacetic Acid → 2-Benzylisonicotinonitrile
https://huagongshe.com/reaction/660033
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetic Acid | HCID 999 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-Cyanopyridine | HCID 7506 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Chlorobenzene water | HCID 19815812 | — |
| Product | 2-Benzylisonicotinonitrile | HCID 13571814 | 61% |
Reaction Steps
p-cyanopyridine (4.00 g, 38.4 mmol) was added to a 1:1 mixture of chlorobenzene/water (750 mL) in a 1 L round-bottom flask. Phenylacetic acid (14.6 g, 107.5 mmol), (NH4)2S2O8 (17.1 g, 74.9 mmol), trifluoroacetic acid (4.38 g, 38.4 mmol) and AgNO3 (0.510 g, 3.0 mmol) were added and the heterogeneous mixture was vigorously stirred at 50° C. 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 (1:5 EtOAc/Hexane) to give a brown oil (4.480 g, 61%); 1H NMR (400 MHz, CDCl3): δ 4.19 (s, 2H), 7.23-7.35 (m, 7H), 8.68 (d, J=5.2 Hz, 1H); 13C NMR (100 MHz, CDCl3): δ 44.4, 120.8, 122.7, 124.6, 126.9, 128.5, 128.9, 129.1, 137.9, 150.2, 162.7; HRMS-EI (m/z): [M+H+] calcd for [C13HN11N2]+, 195.0922. found, 195.0917.
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-075c62eb5be047b49aafec28ed5a27da |
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| Source note | uspto-grants-2011_12 |
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