HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251183Generated: October 26, 2026
Sulfuric Acid → 2,4,5-Trifluorobenzenesulfinic acid
https://huagongshe.com/reaction/2251183
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 2,4,5-Trifluorobenzenesulfonyl chloride | HCID 2776979 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4,5-Trifluorobenzenesulfinic acid | HCID 57241375 | 98.8% |
Reaction Steps
2,4,5-Trifluoro-benzenesulfonyl chloride ([220227-21-4], 2.5 g) was added portionwise onto a solution of sodium sulfite (10.3 g) in 50 mL of water. The reaction mixture was kept under basic conditions by the addition of the proper amount of 20% NaOH and was stirred at room temperature for 1 hour. Methanol was added to the reaction mixture, and the reaction mixture was stirred at room temperature for another hour. After such time, the reaction mixture was cooled down with an ice bath and was then acidified by the addition of 20% H2SO4 solution until reaching pH 2. The aqueous solution was then extracted several times with diethyl ether and ethyl acetate. The aqueous solution was further extracted with ethyl acetate using a Kutscher-Steudel apparatus (continuous extraction). The combined organic phases were dried (sodium sulfate) an concentrated in vacuo to yield the title compound as a white solid (2.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07319099B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-362a4ea739c74b83b6571fd92bc8722b |
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| Source note | uspto-grants-2008_01 |
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