HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849657Generated: October 25, 2026
Carbon Dioxide → 4-(Pentafluoro-lambda6-sulfanyl)benzoic acid
https://huagongshe.com/reaction/849657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Bromo-4-(pentafluoro-lambda6-sulfanyl)benzene | HCID 2779194 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(Pentafluoro-lambda6-sulfanyl)benzoic acid | HCID 2779210 | 35.4% |
Reaction Steps
A solution of n-butyllithium (9.4 ml of a 1.6M solution in hexane) was added to a stirred solution of 4-bromophenylsulphur pentafluoride (3.87 g) in ether at -78° C. under an inert atmosphere. After maintaining at -78° C. for 1 hour, solid carbon dioxide (20 g) was added and the mixture allowed to warm to 5° C. during 1.5 hours. Hydrochloric acid (2M) was added, the mixture stirred for 0.5 hour and the organic phase separated and itself extracted with sodium carbonate solution. The basic extract was washed (ether) and acidified (hydrochloric acid). The precipitated solid was extracted (ether), dried (magnesium sulphate) and evaporated. The residue was triturated (hexane) to give 4-pentafluorosulphanylbenzoic acid as a fawn solid (1.2 g), m.p.188-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06013805 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-66ca446703cd4b58a4e5fa51226ab989 |
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| Source note | uspto-grants-2000_01 |
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