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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171462Generated: November 3, 2026

4-(Trifluoromethyl)aniline → 2-Iodo-4-(trifluoromethyl)aniline

https://huagongshe.com/reaction/1171462

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)anilineHCID 9964—
ReactantIodine chlorideHCID 24640—
SolventMethanolHCID 887—
Product2-Iodo-4-(trifluoromethyl)anilineHCID 278332270.6%

Reaction Steps

To a solution of 4-(trifluoromethyl)benzenamine (10.0 g, 0.0617 mol) in dry methanol (200 ml) was added iodine monochloride (10.49 g, 0.148 mol) in dry MDC (40 ml) at RT slowly. Reaction mixture was stirred at RT over night. The reaction mixture was concentrated, water was added and extracted with ethyl acetate (2×100 ml). The organic layer was washed with water, brine (2×50 ml), dried over Na2SO4 and concentrated. The crude product was purified by column chromatography using 6% ethyl acetate in pet-ether to get 2-iodo-4-(trifluoromethyl)benzenamine (12.5 g, 70%) as pale yellow liquid. 1H NMR (400 MHz, CDCl3) δ 4.42 (bs, 2H), 6.75 (d, 1H), 7.38 (d, 1H), 7.87 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829571B2
Source datasetuspto-grants-2010_11
ORD IDord-f6286e69485a487db77edc1dd4f8161a
Source noteuspto-grants-2010_11