HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2-Cyano-3-phenylprop-2-enoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Isopropyl cyanoacetate | HCID 25917 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Cyano-3-phenylprop-2-enoic acid | HCID 70534 | — |
Reaction Steps
A mixture of 95 g of benzaldehyde, 114.3 g of 7A, 1 g of piperidine and 200 ml of acetic acid was heated on a steam bath for 1 hour. The acetic acid and unreacted benzaldehyde were distilled off, to 100° C./0.2 Torr. The residue was extracted with hot hexane; no residue was left. The solution was chilled, and the solid that formed was recrystallized from methanol to give the 1-methylethyl ester of 2-cyano-3-phenyl-2-propenoic acid (7B), mp: 72°-73° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04235923 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-8db14a2049184cc49281b1470652e865 |
| Source note | uspto-grants-1980_11 |