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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926921Generated: October 28, 2026

Sulfuric Acid → 1,1,1,3,3,3-hexafluoro-2-(2-iodo-5-methylphenyl)propan-2-ol

https://huagongshe.com/reaction/926921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPotassium IodideHCID 4875—
Reactant2-(2-Amino-5-methyl-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-olHCID 320085—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product1,1,1,3,3,3-hexafluoro-2-(2-iodo-5-methylphenyl)propan-2-olHCID 32955571%

Reaction Conditions

Temperature0 °C

Reaction Steps

To compound 1 (2 g, 7.32 mmol) in suspension in distilled water (20 mL) cooled in a ice-bath was added sulfuric acid (0.5 mL). Sodium nitrite (505 mg, 7.32 mmol) dissolved in water (2.5 mL) was added dropwise and another 0.5 mL sulfuric acid was added. The mixture was stirred at 0° C. until complete dissolution of the suspension (ca 30 min). The solution was added dropwise over 30 min to ice cooled potassium iodide (1.46 g, 8.78 mmol) dissolved in distilled water (5 mL). The reaction mixture when then heated at 80° C. until nitrogen formation stops (ca 30 min). After return to room temperature, the red suspension was filtered, washed with water and dissolved in diethylether (50 mL). It was washed with water (20 mL) and 1N hydrochloric acid (20 mL). The organic layer was dried over sodium sulfate and concentrated under vacuum. The residue was chromatographied on a silica gel column with heptane/chloroform (1/1) as eluent to give 1.98 g (5.16 mmol, 71% yield) of a yellow oil which solidifies at 4° C. over night.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290421B2
Source datasetuspto-grants-2016_03
ORD IDord-ab8cf8450fe84f2d941ba39a3c4b91e3
Source noteuspto-grants-2016_03