Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Malonic Acid | HCID 867 | — |
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | p-Cyanocinnamic acid | HCID 86773 | — |
Reaction Steps
0.2mol of p-cyanobenzaldehyde and 0.3mol of malonic acid were dissolved in 80ml of pyridine at room temperature, and 30 drops of piperidine were added thereto. The mixture was heated and stirred for 4 hours at about 100° C. After the reaction, the solution was poured slowly into dilute hydrochloric acid (250ml hydrochloric acid/250g water). Then, the resulting white precipitate was separated by filtering and washed with dilute hydrochloric acid and water, and was recrystallized by use of glacial acetic acid to obtain p-cyanocinnamic acid. 0.3mol of thionyl chloride was added to 0.1mol of the p-cyanocinnamic acid and the mixture was heated and stirred at about 80° C for 3 hours. An excess thionyl chloride was then removed under reduced pressure to obtain p-cyanocinnamic acid chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04058475 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-36ecb62a94a749aa945b12baa3b2cf1e |
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| Source note | uspto-grants-1977_11 |
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