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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401971Generated: October 30, 2026

Sulfuric Acid → 2-Iodo-4-(trifluoromethyl)phenol

https://huagongshe.com/reaction/1401971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant4-(Trifluoromethyl)phenolHCID 67874—
ReactantN-IodosuccinimideHCID 120273—
CatalystN-IodosuccinimideHCID 120273—
SolventAcetic AcidHCID 176—
Product2-Iodo-4-(trifluoromethyl)phenolHCID 11572816242.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-iodosuccinimide (69.5 g, 0.309 moles) was suspended in acetic acid (257 mL) and cooled to 0° C. 4-Trifluoromethylphenol (50.0 g, 0.310 moles) was added followed by sulphuric acid (5.44 mL) dropwise over 5 minutes. The orange-brown suspension was stirred whist warming slowly to room temperature over 18 hours. A further portion of N-iodosuccinimide (2.5 g, 0.011 moles) was added and the mixture was stirred at room temperature for 24 hours. The reaction was quenched by adding water (150 mL) and extracted with dichloromethane (2×100 mL). The combined organics were washed with a saturated aqueous solution of sodium metabisulphite (2×50 mL) and then with saturated aqueous sodium chloride solution (50 mL). The organics were dried over anhydrous magnesium sulphate, filtered and the solvents removed in vacuo to give the crude title product as a light yellow oil. This batch was combined with the products from two further identical reactions and purified by distillation in vacuo. The product was collected boiling at approximately 45° C. at 2 mBar to give the title compound as a pink-orange semi-solid (216 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907101B2
Source datasetuspto-grants-2014_12
ORD IDord-00271aae2ba04235b065c407f4ea2d51
Source noteuspto-grants-2014_12