HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → (1-Butyl-2-oxo-1,2-dihydropyridin-4-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Pyridone | HCID 8871 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Product | (1-Butyl-2-oxo-1,2-dihydropyridin-4-yl)acetic acid | HCID 53429105 | 66% |
Reaction Steps
A solution of pyridinone ix (1.7 g, 10.3 mmol) in 20 mL anhydrous THF is added dropwise to a solution of LDA (2 M, 5.7 mL, 6.05 mmol) in 40 mL anhydrous THF at −78° C. The solution is allowed to stir for 45 minutes followed by the addition of solid CO2 (10 g). After 0.5 h the mixture is poured onto H2O and acidified with 1 N HCl. The solution is concentrated under reduced pressure and extracted with ethyl acetate and CH2Cl2. The combined organics are dried over MgSO4, filtered and concentrated to give a solid which is purified by flash chromatography (9/1:CH2Cl2/MeOH) to provide x as a white solid (1.4 g, 66%). (MS: M+H: 210.0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07589094B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-dc9e87da64d34b028dde1b40045116c7 |
| Source note | uspto-grants-2009_09 |