HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl cyanoacetate → methyl (E)-3-(2,4-dibenzyloxyphenyl)-2-cyanoacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl cyanoacetate | HCID 7747 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2,4-Bis(benzyloxy)benzaldehyde | HCID 1809080 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | methyl (E)-3-(2,4-dibenzyloxyphenyl)-2-cyanoacrylate | HCID 86756581 | — |
Reaction Steps
A mixture of 2,4-dibenzyloxybenzaldehyde (1 g), methyl cyanoacetate (0.27 mL), piperidine (0.1 mL) and ethanol (30 mL) is stirred at ambient temperature for 20 minutes and the solvent is removed under reduced pressure. The residue is recrystallized from ethanol to give methyl (E)-3-(2,4-dibenzyloxyphenyl)-2-cyanoacrylate as a yellow solid (400 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211234B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-c5088d268910443a81fef21ea2bc3c30 |
| Source note | uspto-grants-2001_04 |