HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097232Generated: October 29, 2026
Chloroacetonitrile → HCID 59547214, compound
https://huagongshe.com/reaction/1097232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | 2-Chlorobenzonitrile | HCID 13391 | — |
| Reactant | Sodium selenide | HCID 73973 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59547214 | HCID 59547214 | 44% |
Reaction Steps
To a suspension of sodium selenide (9.14 g, 72.6 mmol, prepared from 5.8 g of selenium as described above) in DMF (72 mL) was added a solution of 2-chlorobenzonitrile (10 g, 72.6 mmol) in DMF (25 mL) at rt for 5 min and stirred the mixture at 100-110° C. for 24 h. Then chloroacetonitrile (5.48 mL, 72.6 mmol) was added dropwise to the reaction mixture and again stirred at 60-70° C. for 2 h. Then, a solution of sodium methoxide (3.9 g, 72.6 mmol) in dry methanol (24 mL) was added dropwise and stirring was continued for 2 h at the same temperature. The mixture was allowed to room temperature (rt) and poured into cold water and stirred for 30 min. The precipitated solid was filtered, washed with water and dried to give the product as an off-white color solid (7 g, 44%), mp 158-160° C. 1H NMR (400 MHz, CDCl3): δ 7.76-7.79 (1H, m, H-7), 7.60-7.63 (1H, m, H-4), 7.41-7.52 (2H, m, H-5,6), 4.90 (2H, br 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-4b1804d194cf4748a7121e9900131e9c |
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| Source note | uspto-grants-2012_03 |
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