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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrisodium PhosphateHCID 24243—
ReactantSodium SulfiteHCID 24437—
Reactant5-Fluoro-2-(trifluoromethyl)benzyl bromideHCID 2737578—
Reactant4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-Fluoro-1-(trifluoromethyl)-2-({[4-(trifluoromethyl)phenyl]sulfonyl}methyl)benzeneHCID 86658724—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609897B2
Source datasetuspto-grants-2013_12
ORD IDord-34b56cd264c3448082cbb593b7fc1165
Source noteuspto-grants-2013_12