HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914254Generated: November 2, 2026
Trisodium Phosphate → 4-Fluoro-1-(trifluoromethyl)-2-({[4-(trifluoromethyl)phenyl]sulfonyl}methyl)benzene
https://huagongshe.com/reaction/1914254
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trisodium Phosphate | HCID 24243 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 5-Fluoro-2-(trifluoromethyl)benzyl bromide | HCID 2737578 | — |
| Reactant | 4-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2777399 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Fluoro-1-(trifluoromethyl)-2-({[4-(trifluoromethyl)phenyl]sulfonyl}methyl)benzene | HCID 86658724 | — |
Reaction Steps
Sodium sulfite (102 g, 809 mmol) was added to sodium phosphate, dibasic (58 g, 409 mmol) and water (550 ml). 4-(trifluoromethyl)benzenesulfonyl chloride (100 g, 409 mmol) and dioxane (65 ml) were then added to the reaction mixture. The reaction was heated to reflux. After 75 min, the reaction was cooled slightly and a solution of 2-trifluoromethyl-5-fluoro-benzyl bromide (75 g, 292 mmol) in ethanol (95 ml) were added and the mixture was refluxed for 1 hr. The reaction was diluted with water (400 ml) and cooled to 0° C. for 1 hr. The reaction mixture was filtered and the solid was washed with water (2×400 ml) and then with heptane (200 ml). The residue was dried under vacuum to a constant weight and carried to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609897B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-34b56cd264c3448082cbb593b7fc1165 |
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| Source note | uspto-grants-2013_12 |
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