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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455335Generated: November 1, 2026

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

https://huagongshe.com/reaction/1455335

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 numberUS07482335B2
Source datasetuspto-grants-2009_01
ORD IDord-6746a74ff1a742b39fbf5e6a8ef6fa05
Source noteuspto-grants-2009_01