HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 3,5-Difluorobiphenyl-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 3,5-Difluorobiphenyl | HCID 13022391 | — |
| Reactant | 1,2,2,3-Tetramethylpiperidine | HCID 18761772 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178418821 | HCID 178418821 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Difluorobiphenyl-4-carboxylic acid | HCID 46314768 | 77% |
Reaction Steps
Dissolve crude 3,5-difluorbiphenyl (1.3 g, 6.83 mmol) in THF (14 mL) and cool to. −78° C. Prepare LiTMP from the addition of BuLi (1.6 M soln in hexanes, 5.33 mL) to tetramethyl piperidine (1.4 mL, 1.25 equiv) at −78° C. in THF (14 mL). Cannulate the cooled LiTMP into the cooled 3,5-difluorobiphenyl and stir the reaction at −78° C. for 1 h. Bubble carbon dioxide gas through the solution for 5 minutes, warm the reaction to rt, pour into 50 mL of 1M NaOB, and extract with 50 mL EtOAc. Discard the organic layer was discarded. Acidify the remaining aqueous layer with conc. HCl and extract twice with EtOAc. Dry the organics over MgSO4, filtered, and evaporate to give 1.22 g of the title compound as a white solid (77%). MS (m/e): 233.1 (M−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07326731B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-91a66127e69f454ebb20ae79a1a0f2f3 |
| Source note | uspto-grants-2008_02 |