HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897586Generated: October 30, 2026
Sodium Carbonate → 2-Chloro-4-(5-fluoro-4-formylpyridin-3-yl)benzonitrile
https://huagongshe.com/reaction/1897586
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Bromo-5-fluoropyridine-4-carboxaldehyde | HCID 53429192 | — |
| Reactant | 2-Chloro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile | HCID 57926113 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Chloro-4-(5-fluoro-4-formylpyridin-3-yl)benzonitrile | HCID 86674838 | 18% |
Reaction Steps
To the solution of 2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (264 mg, 1.00 mmol), 3-bromo-5-fluoroisonicotinaldehyde (204 mg, 1.00 mmol) and PdCl2(PPh3)2 (56 mg, 0.08 mmol) in DMF (3 mL) was added 2M Na2CO3 solution (1.50 ml, 3.00 mmol) under nitrogen atmosphere. The mixture was stirred and heated at 100° C. for 4 hrs. After letting cool to room temperature, solvent was removed in vacuo. The resulting residue was dissolved in DCM and saturated NH4Cl solution. After extraction and separation, the combined extracts were concentrated and purified by SNAP10 g (10% MeOH/DCM 0-15% gradient) to give 2-chloro-4-(5-fluoro-4-formylpyridin-3-yl)benzonitrile (47 mg, 18%) as a white solid; ESI-MS m/z: 293 [M+MeOH+1]+, Retention time 1.15 min. 1H-NMR (CDCl3, 400 MHz) δ 7.33 (dd, J=8.0, 1.6 Hz, 1H), 7.50 (d, J=1.6 Hz, 1H), 7.78 (d, J=8.0 Hz, 1H), 8.49 (s, 1H), 8.78 (d, J=1.2 Hz, 1H), 10.27 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08519134B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-5060bd4428a94798a8e2c37274ca53e6 |
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| Source note | uspto-grants-2013_08 |
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