HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 53726019, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | Hydracrylonitrile | HCID 8011 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 23004044 | HCID 23004044 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 53726019 | HCID 53726019 | — |
Reaction Steps
5-(5-Methoxypentanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione was heated with 3-hydroxypropionitrile (2.79 g, 39.2 mmol) at 80° C. until no more CO2 was released. After cooling to room temperature, the mixture was diluted with 50 ml of 2-propanol and 4-nitrobenzaldehyde (5.40 g, 35.6 mmol), piperidine (150 mg, 1.78 mmol) and acetic acid (110 mg, 1.78 mmol) was added, the mixture was stirred at room temperature for 48 hrs. After evaporation of solvent, the product was purified by chromatography (SiO2, MeOH:CHCl2=5:95). 7-Methoxy-2-[(4-nitrophenyl)methylene]-3-oxoheptanoic acid 2-cyanoethyl ester was obtained as a pale-yellow oil (7.75 g, 60% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608086B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-52ef319784c644f19fa5b05d1ae818e5 |
| Source note | uspto-grants-2003_08 |