HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 2,6-Difluoro-4-pentylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1,3-Difluoro-5-pentylbenzene | HCID 15751978 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,6-Difluoro-4-pentylbenzoic acid | HCID 19010179 | — |
Reaction Steps
A solution of n-butyllithium (10.5M in hexane; 2.70 ml, 0.028 mol) was added dropwise to a stirred, cooled (-78° C.) solution of compound 13 (5.10 g, 0.028 mol) in dry THF (30 ml) under dry nitrogen. The stirred mixture was maintained under these conditions for 2.5 h and then poured onto a slurry of solid carbon dioxide and dry ether. The product was extracted into 10% sodium hydroxide which was then acidified with 36% hydrochloric acid. The acidic mixture was washed with ether (twice), and the combined ethereal layers were washed with water and dried (MgSO4). The solvent was removed in vacuo to yield a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05156763 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-eecfd88f3d4945319632e1940c5c7162 |
| Source note | uspto-grants-1992_10 |