HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722028Generated: October 27, 2026
Carbon Dioxide → p-Toluic acid, 2,3,5,6-tetrafluoro-
https://huagongshe.com/reaction/1722028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3,5,6-Tetrafluorotoluene | HCID 78896 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethoxymethane | HCID 8020 | — |
| Product | p-Toluic acid, 2,3,5,6-tetrafluoro- | HCID 69548 | — |
Reaction Steps
A solution of n-butyllithium (2.7M in n-hexane, 21 cm3) was added dropwise to a stirred solution of 2,3,5,6-tetrafluorotoluene (9.0 g) in dry dimethoxymethane cooled to -70° C. under a nitrogen atmosphere and the mixture stirred for one hour. Carbon dioxide was then passed into the mixture for 3 hours during which time a white solid precipitate formed. After allowing the mixture to attain the ambient temperature (ca. 22° C.) it was poured into water. The resultant mixture was acidified with dilute hydrochloric acid and extracted with diethyl ether. The ethereal extract was washed with water and dried over anhydrous magnesium sulphate. Removal of the solvent yielded a semi solid residue which on trituration with petroleum ether (boiling range 40°-60° C.) gave 4-methyl-2,3,5,6-tetrafluorobenzoic acid (2.5 g) white crystals, mp 168° C. (Infra red C=O, 1700 cm-1.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853414 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-15ad55d882074257918a81a38fc4eb73 |
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| Source note | uspto-grants-1989_08 |
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