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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416698Generated: October 31, 2026

Triethylamine → HCID 22632168, compound

https://huagongshe.com/reaction/2416698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethyl)benzylamineHCID 76804—
Reactant2-Bromo-5-methoxybenzyl bromideHCID 3525951—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22632168HCID 2263216873.1%

Reaction Steps

To a stirred solution of 4-bromo-3-bromomethylanisole (35 g, 125 mmol) in anhydrous DMSO (50 mL) and dry THF (50 mL) was added 4-trifluoromethylbenzylamine (30 g, 171 mmol) followed by triethylamine (18 mL, 129 mmol). After stirring for 18 h at RT the reaction was concentrated, diluted with aqueous 1 N NaOH (250 mL) and extracted with Et2O (2×250 mL). The combined organic layers were washed with brine, dried (Na2SO4), and concentrated to dryness. The residue which remained was purified by flash chromatography on silica gel (10 to 20% EtOAc/CHCl3) to give the title compound (34.17 g, 73%): TLC (20% EtOAc/CHCl3) Rf 0.63; 1H NMR (400 MHz, CDCl3) δ 7.59 (d, J=8.2 Hz, 2H), 7.49 (d, J=8.2 Hz, 2H), 7.43 (d, J=8.6 Hz, 1H), 6.96 (d, J=3.1 Hz, 1H), 6.70 (dd, 1H), 3.86 (s, 2H), 3.84 (s, 2H), 3.79 (s, 3H), 1.75 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825188B2
Source datasetuspto-grants-2004_11
ORD IDord-2d7cc7ab4323485bba24b7bad02a01f2
Source noteuspto-grants-2004_11