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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028636Generated: October 30, 2026

Iodine → 2-iodine-4 -(trifluoromethyl) anisole

https://huagongshe.com/reaction/1028636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTert-Butyl nitriteHCID 10906—
Reactant2-Methoxy-5-(trifluoromethyl)anilineHCID 600637—
SolventDichloromethaneHCID 6344—
Product2-iodine-4 -(trifluoromethyl) anisoleHCID 18706296—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of 2-methoxy-5-(trifluoromethyl)aniline (500 mg, 2.62 mmol) in CH2Cl2 (10 mL) was added t-butyl nitrite (467 μL, 3.93 mmol). The reaction was stirred for 5 min prior to addition of iodine (1.3 g, 5.24 mmol), and then heated at 70° C. for 2 h. The reaction was cooled, diluted with CH2Cl2 (10 mL), washed with sat. Na2S2O3 (10 mL) and brine (10 mL), dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash silica gel chromatography (hexanes) to afford 2-iodo-1-methoxy-4-(trifluoromethyl)benzene as a light yellow solid. 1H NMR (CDCl3, 500 MHz): δ 8.05 (d, J=2 Hz, 1 H), 7.61 (dd, J=8.7, 1.8 Hz, 1 H), 6.89 (d, J=8.7 Hz, 1 H), 3.97 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735435B2
Source datasetuspto-grants-2014_05
ORD IDord-c46a75d80afd45b0b757b068b936273c
Source noteuspto-grants-2014_05