HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097230Generated: October 31, 2026
Chloroacetonitrile → HCID 86646892, compound
https://huagongshe.com/reaction/1097230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium selenide | HCID 73973 | — |
| Reactant | 2-Chloronicotinonitrile | HCID 81079 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86646892 | HCID 86646892 | 81.3% |
Reaction Steps
To a suspension of sodium selenide (0.9 g, 7.2 mmol, prepared from 0.75 g of selenium as described above) in DMF (7 mL) was added a solution of 2-chloropyridine-3-carbonitrile (1 g, 7.2 mmol) in DMF (3 mL) at rt for 5 min and stirred the mixture at 60-70° C. for 2 h. Then chloroacetonitrile (0.46 mL, 7.22 mmol) was added dropwise to the reaction mixture and again stirred at 60-70° C. for 2 h. Then, a solution of sodium methoxide (0.39 g, 7.2 mmol) in methanol (7 mL) was added dropwise and stifling was continued for 1 h at the same temperature. The mixture was allowed to room temperature (rt) and poured into cold water and stirred for 15 min. The precipitated solid was filtered, washed with water and dried to give the product as a yellow color solid (1.3 g, 81%), mp 208-210° C. 1H NMR (400 MHz, DMSO-d6): δ 8.68 (1H, d, J=4.4 Hz, H-6), 8.47 (1H, d, J=8.4 Hz, H-4), 7.55 (1H, dd, J=8.0, 4.8 Hz, H-5), 7.24 (2H, s, —NH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143237B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-6a6c8fde7a79445db5228b56143c76f8 |
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| Source note | uspto-grants-2012_03 |
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