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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382088Generated: November 3, 2026

Allyl bromide → Allyl-(2-iodo-4-trifluoromethyl-phenyl)-amine

https://huagongshe.com/reaction/2382088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTetrahydrofuranHCID 8028—
Reactant2-Iodo-4-(trifluoromethyl)anilineHCID 2783322—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
ProductAllyl-(2-iodo-4-trifluoromethyl-phenyl)-amineHCID 6855534033.4%

Reaction Steps

To a mixture of 2-iodo-4-trifluoromethyl-aniline (5 g, 17.4 mmol), KOt-Bu (2.05 g, 18.3 mmol) and THF (200 mL) at −78° C., is added allyl bromide (2.21 g, 18.3 mmol). The resulting mixture is warmed to rt and stirred for 18 h. Water is added, and the mixture is extracted with EtOAc. The organic layer is separated, dried (Na2SO4), filtered and concentrated. The residue is chromatographed through silica gel eluting with 0-50% EtOAc in heptane to afford allyl-(2-iodo-4-trifluoromethyl-phenyl)-amine (1.9 g, 33%). MS 328 (M+H); 1H NMR (300 MHz, CDCl3): δ 7.90 (s, 1H), 7.45 (d, 1 H), 5.88-6.02 (m, 1H), 5.33 (d, 1 H), 5.25 (d, 1H), 4.72(broad s, 1H), 3.90 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-6a2e71c1b9b941e8ab0246ec49293e3f
Source noteuspto-grants-2012_09