HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2,2-Dimethyl-3-oxo-5-pyridin-4-yl-pent-4-enenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Reactant | 2,2-Dimethyl-3-oxobutanenitrile | HCID 12468309 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,2-Dimethyl-3-oxo-5-pyridin-4-yl-pent-4-enenitrile | HCID 69137649 | 59% |
Reaction Steps
Pyridine-4-carboxaldehyde (6.9 ml, 72 mmol) was added to dry pyridine (16 ml) under argon. 2,2-Dimethyl-3-oxo-butyronitrile {J. K. Rasmussen et al., Synthesis, 1973, 682} (8.0 g, 72 mmol) and diethylamine (7.3 ml, 71 mmol) were subsequently added and the solution heated under reflux for 18 hours. After cooling to room temperature, the mixture was poured into water and ethyl acetate. The mixture was separated and the aqueous phase re-extracted with ethyl acetate. The combined organic layers were dried and concentrated in vacuo to yield a solid which was triturated with diethyl ether to give the title compound (8.5 g, 59%); MS (ES+) m/e 201 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375105B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-d5300a5ebe9c40e7a60c0c58261e9f58 |
| Source note | uspto-grants-2008_05 |