HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl cyanoacetate → 2-cyano-N-(4-methylbenzyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | 4-Methylbenzylamine | HCID 66035 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 2-cyano-N-(4-methylbenzyl)acetamide | HCID 903339 | — |
Reaction Steps
A solution of 93 g. (0.825 mole) of ethyl cyanoacetate and 100 g. (0.825 mole) of 4-methylbenzylamine in 150 ml. of 2-methoxyethanol is refluxed for 2 hr. After cooling the solid product is isolated by vacuum filtration, washed with pentane and dried to give 90 g. (57.6%) of amide as a white solid: m.p. 124°-6° C.; ν 3220 (NH), 2230 (CN), and 1630 cm.-1 (C=O) δ 8.77 broad, 1H, NH); 7.17 (s, 4H, phenyl protons), 4.28 (d, 2H, benzyl methylene), 3.67 (s, 2H, CH2CO), and 2.28 (s, 3H, CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028084 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-1dc9e47af7dd4db8b708c359080e8de4 |
| Source note | uspto-grants-1977_06 |