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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225148Generated: October 31, 2026

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

https://huagongshe.com/reaction/2225148

Reaction equation

Participants

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

Reaction Steps

Preparation B5, Step 1: 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 numberUS07378409B2
Source datasetuspto-grants-2008_05
ORD IDord-f8aae3d70b734704b41f13ed58978434
Source noteuspto-grants-2008_05