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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174433Generated: October 31, 2026

Hydrogen Bromide → Quinoline

https://huagongshe.com/reaction/1174433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantHCID 21111652HCID 21111652—
SolventAcetic AcidHCID 176—
ProductQuinolineHCID 704729.2%

Reaction Steps

The 5-trifluoromethyl-8-methoxyquinoline 8.50 g was dissolved in 100 mL glacial acetic acid and added to 20 ml HBr in a 100 mL flask. The solution was heated to reflux for 20 hrs. The reaction mixture was allowed to come to room temperature. The reaction mixture was concentrated by removal of 55 mL of solvent under vacuum. The solution was then poured into 100 mL cold water and neutralized with 2N NaOH to pH 7.0. The resulting solution was extracted with 2×100 ml ether, dried with NaSO4, filtered and concentrated to an oil, which solidified upon standing (5.0 g). The crude material was purified by filtration through a short silica gel column where the silica was first washed with 2% TEA in methylene chloride. The column was then dried under N2 pressure and re-solvated with neat methylene chloride. Elution with 2% EtOH/methylene chloride gave 1.41 g of the desired product as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838127B1
Source datasetuspto-grants-2010_11
ORD IDord-40cb68acbd7d4de4bfce8a56b3b3ff72
Source noteuspto-grants-2010_11