HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 54398794, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | HCID 14627908 | HCID 14627908 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54398794 | HCID 54398794 | 75.8% |
Reaction Steps
o-Nitrobenzaldehyde (7.6 g, 0.05 mole) and acetoacetic cyclopropylamide (7.1 g, 0.05 mole) are dissolved in benzene (40 ml) and thereto are added piperidine (0.2 ml) and acetic acid (0.6 ml), and the mixture is refluxed for 2 hours and the produced water is removed. After the stoichiometic amount of water is distilled off, the reaction is stopped. After the reaction, the reaction mixture is washed with 5% hydrochloric acid and then with water, and the solvent is distilled off under reduced pressure, and to the residue is added diethyl ether, and the obtained crude crystals are recrystallized from ethanol to give the title compound (10.4 g, yield 75.6%) as colorless needles, m.p. 133°-134° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04874773 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-2014cf112da144f08d20489e2b7da7ed |
| Source note | uspto-grants-1989_10 |