HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrobenzaldehyde → HCID 68120470, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Diethyl oxalacetate | HCID 66951 | — |
| Reactant | HCID 45122131 | HCID 45122131 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68120470 | HCID 68120470 | — |
Reaction Steps
After heating a solution of 15.1 g of 3-nitrobenzaldehyde, 16 g of β-amino-γ-methoxycrotonic acid ethyl ester and 19 g of oxalacetic acid diethyl ester in 60 ml of ethanol under reflux for 12 hours, the mixture is evaporated in vacuo and 2-methoxymethyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-3,5,6-tricarboxylic acid triethyl ester is obtained in almost quantitative yield, in the form of a yellow oil (nD50 =1.5353).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04020178 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-8011c251fe7e4477807065bc1004edc4 |
| Source note | uspto-grants-1977_04 |