HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 5-Bromo-2,3,4-trifluorobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-Bromo-2,3,4-trifluorobenzene | HCID 2733255 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 5-Bromo-2,3,4-trifluorobenzoic acid | HCID 11118637 | — |
Reaction Steps
To a solution of 2,3,4-trifluorobromobenzene in appropriate solvent is added strong base (such as LDA, nBuLi, LiHDMS) under nitrogen atmosphere. The reaction is generally carried out at low temperature (−50-−80° C., prefer −78° C.). The reaction is kept stirring for some time (0.5-12 h, preferably select 0.5-2 h) and is added dry ice. The resulting mixture is kept stirring for some time (3-12 h, prefer 5-10 h) and 5-bromo-2,3,4-trifluorobenzoic acid is obtained after conventional workup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290468B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-1512aeb100d442a7a5e4265785457d96 |
| Source note | uspto-grants-2016_03 |