HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl cyanoacetate → Ethyl 3-(4-chloro-3-fluorophenyl)-2-cyanoacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Chloro-3-Fluorobenzaldehyde | HCID 2724985 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 3-(4-chloro-3-fluorophenyl)-2-cyanoacrylate | HCID 67338173 | 88% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
4-Chloro-3-fluorobenzaldehyde (1.0 g, 6.3 mmol) was added to a solution of ethyl 2-cyanoacetate (0.71 g, 6.3 mmol) and piperidine (0.081 ml, 0.82 mmol) in toluene (10 mL) at room temperature. The mixture was heated at 100° C. for 7 hours. Upon cooling to room temperature, the mixture was concentrated in vacuo and rinsed with hexane to give ethyl 3-(4-chloro-3-fluorophenyl)-2-cyanoacrylate (1.4 g, 88%). LCMS (APCI+) [M+H]+ 253.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08003651B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-63ac80f4255645b9b0a522370885bdb5 |
| Source note | uspto-grants-2011_08 |