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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17063Generated: October 25, 2026

Iodine → 1-Iodo-3-methoxy-5-(trifluoromethyl)benzene

https://huagongshe.com/reaction/17063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTert-Butyl nitriteHCID 10906—
Reactant5-(Trifluoromethyl)-m-anisidineHCID 605671—
ReactantSodium BisulfiteHCID 23665763—
SolventChloroformHCID 6212—
Product1-Iodo-3-methoxy-5-(trifluoromethyl)benzeneHCID 19773106—

Reaction Conditions

Temperature50 °C

Reaction Steps

3-methoxy-5-(trifluoromethyl)aniline (100 mg, 0.52 mmol) was dissolved in CHCl3 (5.2 mL) and t-butyl nitrite (124 μL, 1.05 mmol) was added dropwise by syringe. Iodine (266 mg, 1.05 mmol) was added and then the reaction was slowly heated to 50° C. and was maintained at this temperature for an hour and thirty minutes. The reaction was then cooled to room temperature and poured into aq. NaHSO3 (50 mL). The mixture was extracted with EtOAc (50 mL) and the organic extracts were washed with aq. NaHSO3 (3×50 mL) and brine (20 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 1% to 15% EtOAc/hexanes afforded 1-iodo-3-methoxy-5-(trifluoromethyl)benzene. Rf=0.75 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 7.53 (s, 1H), 7.41 (s, 1H), 7.09 (s, 1H), 3.82 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737295B2
Source datasetuspto-grants-2010_06
ORD IDord-af5aad6c0b7141c09bdc994dbba30573
Source noteuspto-grants-2010_06