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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550882Generated: October 25, 2026

Hydrogen Bromide → 7-Trifluoromethyl-4-(beta-bromoethylamino)quinoline

https://huagongshe.com/reaction/550882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSulfuric AcidHCID 1118—
ReactantSodium BicarbonateHCID 516892—
Reactant2-((7-(Trifluoromethyl)quinolin-4-yl)amino)ethanolHCID 67187791—
SolventWaterHCID 962—
Product7-Trifluoromethyl-4-(beta-bromoethylamino)quinolineHCID 6718989258%

Reaction Conditions

Temperature165 °C

Reaction Steps

Hydrobromic acid (0.88 ml, 16.2 mmol) and then sulphuric acid (0.29 ml, 5.5 mmol) are added dropwise to the 7-trifluoromethyl-4-(β-hydroxyethylamino)quinoline 10 (0.67 g, 2.6 mmol), the reaction medium being refrigerated using a bath of cold water. The reaction medium is then heated at 165° C. for 3 h 30 min, and then poured into 10 ml of cold water. The pH is then adjusted by adding NaHCO3 (pH approximately 9) and the medium is then extracted at the reflux of toluene (10 ml) for 15 min. The organic phase is then collected and the product 11 is obtained by crystallization at −18° C. overnight, filtration, and then drying under vacuum: 0.48 g (yield=58%). Mp: 106° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947701B2
Source datasetuspto-grants-2011_05
ORD IDord-cff83e05c5c6482ab78021e4add0cbd7
Source noteuspto-grants-2011_05