HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 86586634, 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 23004045 | HCID 23004045 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86586634 | HCID 86586634 | — |
Reaction Steps
5-(6-Azidohexanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione was heated with 3-hydroxypropionitrile (8.90 g, 125 mmol) at 80° C. until no more CO2 was released. The reaction mixture was diluted with 150 ml of 2-propanol and 4-nitrobenzaldehyde (6.30 g, 41.7 mmol), piperidine (178 mg, 2.10 mmol) and acetic acid (125 mg, 2.10 mmol) were added. The mixture was stirred at room temperature for 48 hrs. After the solvent was evaporated, the residue was dissolved into CHCl3 (200 ml), washed with water (150 ml) and brine (150 ml). After drying (Na2SO4) and evaporation of solvent, 8-azido-2-[ (4-nitrophenyl)methylene]-3-oxooctanoic acid 2-cyanoethyl ester was obtained as a brownish oil (17.0 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211198B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-2a52b47afede4b37912a60232329e390 |
| Source note | uspto-grants-2001_04 |