HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-(3,4-dichlorobenzyl)-2-cyanoacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Benzenemethanamine, 3,4-dichloro- | HCID 1608 | — |
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(3,4-dichlorobenzyl)-2-cyanoacetamide | HCID 4168883 | — |
Reaction Steps
A solution of 113.3 g. (1.002 moles) of ethyl cyanoacetate and 176.4 g. (1.002 moles) of 3,4-dichlorobenzylamine in 400 ml. of absolute ethanol is heated at reflux with stirring for 42 hours which upon cooling the entire solution solidifies. The latter is broken-up, slurried in ether, isolated by filtration and dried in vacuo to give 179.8 g. of product as a white solid, m.p. 144°-5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04028084 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-aad702e175dd404bb99140aa581dbf31 |
| Source note | uspto-grants-1977_06 |