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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042718Generated: October 27, 2026

2-Bromo-5-(trifluoromethyl)benzenamine → 2-(3-Dimethylamino-1-propynyl)-5-(trifluoromethyl)aniline

https://huagongshe.com/reaction/1042718

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-(trifluoromethyl)benzenamineHCID 67989—
ReactantDiisopropylethylamineHCID 81531—
ReactantN,N-DimethylpropargylamineHCID 81643—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product2-(3-Dimethylamino-1-propynyl)-5-(trifluoromethyl)anilineHCID 68463994—

Reaction Steps

A resealable tube was charged with 2-bromo-5-(trifluoromethyl)aniline (1.00 g, 4.16 mmol), 1-dimethylamino-2-propyne (0.520 g, 6.20 mmol), PdCl2(PPh3)2 (0.15 g, 0.21 mmol), copper iodide (0.80 mg, 0.42 mmol), diisopropylethylamine (1.0 mL) and acetonitrile (3.0 mL). The system was purged with argon, the tube sealed and the mixture stirred at room temperature for 20 h. The reaction mixture was filtered through celite and concentrated. The residue was purified via column chromatography on silica gel (gradient elution with 0-10% methanol-dichloromethane) to afford 2-(3-dimethylamino-1-propynyl)-5-(trifluoromethyl)aniline as a brown oil. MS m/z=243 [M+H]+. Calc'd for C12H13F3N2: 242.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557996B2
Source datasetuspto-grants-2013_10
ORD IDord-cc63730451cc41288e6f4395d933f090
Source noteuspto-grants-2013_10