HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333326Generated: October 26, 2026
Piperidine → (E)-tert-butyl 2-cyano-3-(3,4-dichlorophenyl)acrylate
https://huagongshe.com/reaction/333326
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3,4-Dichlorobenzaldehyde | HCID 22710 | — |
| Reactant | tert-Butyl cyanoacetate | HCID 70693 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (E)-tert-butyl 2-cyano-3-(3,4-dichlorophenyl)acrylate | HCID 68751356 | 81.7% |
Reaction Steps
A solution of tert-butyl cyanoacetate (2.52 ml, 17.63 mmol), 3,4-dichlorobenzaldehyde (2.57 g, 14.69 mmol) and piperidine (0.145 ml, 1.469 mmol) in EtOH (50 ml) was allowed to stir at 80° C. for 15 hours, and then cooled to ambient temperature. A half volume of the solvent was evaporated, and 400 ml of water was added to the resulting mixture. The precipitated solid was collected and washed with 5% iPrOH/H2O (200 ml). The solid was dried under reduced pressure to give (E)-tert-butyl 2-cyano-3-(3,4-dichlorophenyl)acrylate (3.577 g); Retention time=1.61 minutes (condition A); MS (ES+)=315.1 (m+18).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08877815B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-1491605790b04672bdfb6bed058d5069 |
|---|
| Source note | uspto-grants-2014_11 |
|---|