HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 7-Azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoic acid 2-cyanoethyl ester
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 | 5-(5-Azidopentanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 23004073 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoic acid 2-cyanoethyl ester | HCID 53869981 | — |
Reaction Steps
5-(5-Azidopentanoyl)-2,2-dimethyl-1,3-dioxane-4,6-dione was heated with 3-hydroxypropionitrile (2.42 g, 34.0 mmol) at 80° C. until no more CO2 was released. After cooling to room temperature, the mixture was diluted with 150 ml of 2-propanol, and 4-nitrobenzaldehyde (4.60 g, 30.3 mmol), piperidine (130 mg, 1.50 mmol) and acetic acid (90 mg, 1.50 mmol) were added. The mixture was stirred at room temperature for 48 hrs. The product, 7-azido-2-[(4-nitrophenyl)methylene]-3-oxoheptanoicacid2-cyanoethyl ester was obtained as a pale-yellow oil (5.73 g, 51% yield) after chromatography (SiO2, Hexane: AcOEt, 2:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211198B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-a7ed828c3a644913b50194ade03649ce |
| Source note | uspto-grants-2001_04 |