HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097213Generated: October 28, 2026
Ethyl chloroacetate → HCID 59547216, compound
https://huagongshe.com/reaction/1097213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| 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 59547216 | HCID 59547216 | 77.4% |
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 ethyl chloroacetate (0.78 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 stirring 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 (1.5 g, 77%), mp 194-196° C. 1H NMR (400 MHz, CDCl3): δ 8.65 (1H, dd, J=4.6, 1.4 Hz, H-6), 7.86 (1H, dd, J=8.2, 1.4 Hz, H-4), 7.33 (1H, dd, J=8.2, 4.6 Hz, H-5), 6.04 (2H, br s, —NH2), 4.34 (2H, q, J=7.1 Hz, —COOCH2CH3), 1.38 (3H, t, J=7.1 Hz, —COOCH2CH3); LC-MS (positive ion mode): m/z 269, 271 (M+H)+.
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-fa60355edf2645deb10a71f8da756b7e |
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| Source note | uspto-grants-2012_03 |
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