HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → Benzyl 2-[(2-nitrophenyl)methylidene]-3-oxobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | Benzyl acetoacetate | HCID 142266 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Benzyl 2-[(2-nitrophenyl)methylidene]-3-oxobutanoate | HCID 54323135 | 107.9% |
Reaction Steps
A mixture of 2-nitrobenzaldehyde (3.023 g), benzyl acetoacetate (3.802 g) and piperidine (272.5 mg) in benzene (10 ml), was treated in a substantially similar manner that of Example 1-11) to give a brown oil (6.94 g) of benzyl 2-(2-nitrobenzylidene)acetoacetate, which was further treated with ethyl 3-amino-4,4-diethoxycrotonate (4.34 g) to give a dark brown oil (10.3 g). This oil was purified by column chromatography on silica-gel and the resultant oil (3.8 g) was crystallized to give crystals (1.65 g) of benzyl 2-methyl-4-(2-nitrophenyl)-5-ethoxycarbonyl-6-diethoxymethyl-1,4-dihydropyridine-3-carboxylate, m.p. 103° to 103.5° C. (recrystallized from a mixture of diisopropyl ether and n-hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04370334 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-8aeeee6144c54592b79652c9cf7587e4 |
| Source note | uspto-grants-1983_01 |