HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 6-Fluoro-2,4-dimethyl-nicotinic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 3-Bromo-6-fluoro-2,4-dimethylpyridine | HCID 68973514 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 6-Fluoro-2,4-dimethyl-nicotinic acid | HCID 68775351 | 73% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a solution of 3-bromo-2,4-dimethyl-6-fluoropyridine (1.45 g, 7.10 mmol) in anhydrous Et2O (25 mL) at −78° C. was added t-BuLi (1.7M in pentane, 8.8 mL, 15 mmol) dropwise. After addition the mixture was stirred at −78° C. for 10 min, and CO2 was introduced. After 10 min the cooling bath was removed, and the bubbling of CO2 was continued until the mixture was warmed to 0° C. Water (30 mL) was then added and Et2O was removed. The aqueous layer was washed CH2Cl2 (2×30 mL) and acidified with 6N HCl, resulting in precipitation of a pale brown solid (0.87 g, 73%) which was collected by filtration and dried under vacuum. 1H NMR (CD3OD): δ 2.38 (s, 3H), 2.46 (s, 3H), 6.69 (s, 1H). 19F NMR (CD3OD): δ 0.63.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07498346B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-530c13a757684a41ba0314864b7f377d |
| Source note | uspto-grants-2009_03 |