HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl cyanoacetate → HCID 11659490, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Cyclopropyl methyl ketone | HCID 13004 | — |
| Reactant | 3,4-Dichlorobenzaldehyde | HCID 22710 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11659490 | HCID 11659490 | — |
Reaction Steps
While being stirred, 300 ml of ethanol is mixed with 14 g of acetyl cyclopropane, 18 g of cyanoacetic acid ethyl ester, 28 g of 3,4-dichlorobenzaldehyde as well as 100 g of ammonium acetate, and it is subsequently heated to boiling for six hours at a bath temperature of 80-90° C. After some length of time, a portion of the product already precipitates from the reaction solution. To complete the precipitation, it is then allowed to cool to room temperature while being stirred. The precipitate is suctioned off, washed acetate-free with cold ethanol and water and ultimately dried. 15 g of product accumulates, melting point 290-295° C., while decomposing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977325B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-d6ba8dd1e4d849b3b423d4dad5dd7d55 |
| Source note | uspto-grants-2011_07 |