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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46399Generated: October 25, 2026

Iodine → 5-Fluoro-2-iodo-4-(trifluoromethyl)phenol

https://huagongshe.com/reaction/46399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantChloroformHCID 6212—
Reactant3-Fluoro-4-(trifluoromethyl)phenolHCID 2774800—
CatalystSilver trifluoroacetateHCID 76299—
Product5-Fluoro-2-iodo-4-(trifluoromethyl)phenolHCID 5943649655.7%

Reaction Steps

A solution of iodine (0.874 g, 3.44 mmol) in chloroform (17.1 mL, 214 mmol) was added over a period of 1.5 hours dropwise via addition funnel to a mixture of 3-fluoro-4-(trifluoromethyl)phenol (Preparation 886, 620 mg, 3.4 mmol) and silver trifluoroacetate (0.760 g, 3.44 mmol) in chloroform (3.4 mL, 43 mmol). After addition was complete, the reaction mixture was stirred an additional 1 hour. The reaction mixture was filtered through diatomaceous earth, and the filtrate was washed successively with 10% aqueous sodium thiosulfate (w/v), half-saturated aqueous sodium bicarbonate, water and brine. The organic phase was dried over sodium sulfate, filtered, and concentrated onto diatomaceous earth. The residue was purified by automated flash chromatography (24 g SiO2, hexanes to 1:1 methylene chloride-hexanes gradient elution). The initial product-containing fraction contained predominantly diiodinated material (by mass) with some monoiododinated material. The remaining fractions were concentrated in vacuo to afford the product as a light yellow oil (579 mg, 54%). The product was not dried under vacuum due to volatility.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541588B2
Source datasetuspto-grants-2013_09
ORD IDord-43cb9afef6fd4e369f6691015b6df7f0
Source noteuspto-grants-2013_09