HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904592Generated: October 31, 2026
Carbon Dioxide → 4-Bromo-2,3,5,6-tetrafluorobenzoic acid
https://huagongshe.com/reaction/1904592
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dibromo-2,3,5,6-tetrafluorobenzene | HCID 67653 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Bromo-2,3,5,6-tetrafluorobenzoic acid | HCID 298173 | 81.5% |
Reaction Steps
n-Butyllithium (42 ml, 2.4M in hexane) was slowly added to a solution of 30.78 g 1,4-dibromo-2,3,5,6-tetrafluorobenzene in 200 ml tetrahydrofuran cooled to -70° C. under nitrogen. Solid carbon dioxide (about 12 g) was then added to the stirred mixture which was then allowed gradually to warm to 0° C. at which point 16 ml 6M hydrochloric acid and 16 ml water were added. The reaction mixture was concentrated and the residue extracted with methylene dichloride. The extract was washed with concentrated sodium chloride solution, dried (magnesium sulfate) and concentrated to dryness to give 22.23 g (81.5%) 4-bromo-2,3,5,6-tetrafluorobenzoic acid, m.p. 128°-135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04839355 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-5afd748ed2ad428e99eb49f2f1d2eef7 |
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| Source note | uspto-grants-1989_06 |
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