HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Chloroethyl 2-[(2-nitrophenyl)methylidene]-3-oxobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | 2-Chloroethyl acetoacetate | HCID 108605 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Chloroethyl 2-[(2-nitrophenyl)methylidene]-3-oxobutanoate | HCID 54072926 | — |
Reaction Steps
A mixture of 2-nitrobenzaldehyde (4.536 g), 2-chloroethyl acetoacetate (4.94 g) and piperidine (110 mg) in benzene (18 ml) and acetic acid (360 mg) was refluxed for an hour under azeotropic dehydration. The reaction mixture was washed with water and dried. The solvent was distilled off to give an reddish oil of 2-chloroethyl 2-(2-nitrobenzylidene)acetoacetate, and thus obtained oil was treated with ethyl 3-amino-4,4-diethoxycrotonate (7.1 g) to give yellow granules of 2-chloroethyl 2-methyl-4-(2-nitrophenyl)-5-ethoxycarbonyl-6-diethoxymethyl-1,4-dihydropyridine-3-carboxylate, m.p. 82° to 84° C. (recrystallized from diisopropyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04370334 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-5640841311764ae6be452d3f1931f7fb |
| Source note | uspto-grants-1983_01 |