HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl cyanoacetate → HCID 53653792, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Ethyl (4-formyl-2-methoxyphenoxy)acetate | HCID 968872 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53653792 | HCID 53653792 | 93.9% |
Reaction Steps
A mixture of 4-carbethoxymethoxy-3-methoxybenzaldehyde (23.8 g, 0.10 mol), ethyl cyanoacetate (11.3 g, 0.10 mol), ethanol (150 mL) and piperidine (2 mL) is heated at reflux for 4 hours. The reaction mixture is allowed to cool, and the solid is collected by filtration, washed with ethanol and dried in air. A yield of 31.3 g (93%) of product is obtained which has the following structure as supported by mass spectrometry: ##STR21## An absorption maximum at 355 nm is observed when the product is dissolved in methylene chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05215876 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-9b7f2899ada443eeb6acbbc363b24b82 |
| Source note | uspto-grants-1993_06 |