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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401998Generated: October 27, 2026

Sulfuric Acid → 4-(Difluoromethoxy)-2-iodophenol

https://huagongshe.com/reaction/1401998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantN-IodosuccinimideHCID 120273—
Reactant4-(Difluoromethoxy)phenolHCID 2774124—
SolventAcetic AcidHCID 176—
SolventCitric AcidHCID 311—
SolventWaterHCID 962—
Product4-(Difluoromethoxy)-2-iodophenolHCID 5943654642%

Reaction Steps

To a suspension of N-iodosuccinimide (1.12 g, 0.005 mol) in acetic acid (15.0 mL) was added 4-(difluoromethoxy)phenol (0.8 g, 0.005 mol) under nitrogen. Sulfuric acid (0.147 g, 0.0015 mol) was added and the resulting dark brown suspension was stirred at room temperature for 4 hours before the addition of N-iodosuccinimide (0.6 g, 0.0025 mol). The mixture was stirred for 16 hours before diluting with citric acid (1.0 M aqueous solution, 20.0 mL) and water (20.0 mL). The aqueous layer was extracted with dichloromethane (2×30.0 mL). Combined organic layers were dried over sodium sulphate, filtered and concentrated in vacuo to afford a dark purple oil. This was concentrated in vacuo from toluene (3×20.0 mL) to afford a brown oil. The aqueous layer was concentrated in vacuo. Both organic and aqueous crude residues were purified by flash column chromatography on the ISCO™ (40 g SiO2) eluting with ethyl acetate:heptane (gradient 0:1 to 1:1, by volume) to afford the title compound as a yellow oil, 0.604 g, 42% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907101B2
Source datasetuspto-grants-2014_12
ORD IDord-312242b697d945d0ad77c840d28e9223
Source noteuspto-grants-2014_12