HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 54471283, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Benzaldehyde, 4-[2-[2-(2-chlorophenyl)-5-methyl-4-oxazolyl]ethoxy]- | HCID 10991479 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54471283 | HCID 54471283 | 96% |
Reaction Steps
A mixture of 4-[2-[2-(2-chlorophenyl)-5-methyl-4-oxazolyl]ethoxy]benzaldehyde (2.0 g), ethyl cyanoacetate (0.795 g), piperidine (0.15 g) and pyridine (30 ml) was stirred for 2 hours at 100°-110° C. The reaction mixture was poured into water. Resulting crystalline precipitate was collected by filtration and recrystallized from dichloromethane-ethanol to give ethyl 4-[2-[2-(2-chlorophenyl)-5-methyl-4-oxazolyl]ethoxy]-α-cyanocinnamate (2.45 g, 96%) as colorless needles, m.p.120°-121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05591862 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-4fd84f3a4204497a93df2c2c964b1741 |
| Source note | uspto-grants-1997_01 |