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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098037Generated: October 31, 2026

Ethyl Acetate → 5-Bromo-3-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/2098037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantN-bromobutanimideHCID 67184—
Reactant3-(Trifluoromethyl)quinolineHCID 12025166—
SolventSulfuric AcidHCID 1118—
SolventSodium SulfiteHCID 24437—
Product8-Bromo-3-(trifluoromethyl)quinolineHCID 46941511—
Product5-Bromo-3-(trifluoromethyl)quinolineHCID 6875901437%

Reaction Steps

3-(Trifluoromethyl)quinoline (7.00 g, 35.5 mmol) and N-bromosuccinimide (9.00 g, 50.6 mmol) in concentrated sulfuric acid (50 ml) was heated to 50° C. After stirring for 1.5 h, the solution was cooled to ambient temperature, diluted with saturated aq. sodium sulfite, made alkaline with 3 N aq. sodium hydroxide, and extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was flash chromatographed with 99:1, 49:1, 24:1, and 23:2 hexane:ethyl acetate as the eluant to afford 4.55 g of impure 8-bromo-3-(trifluoromethyl)quinoline and 3.89 g (37% yield) of 5-bromo-3-(trifluoromethyl)quinoline. Method [8] Retention time 6.75 and 7.47 min by HPLC (M+=276 and 278) and (M+=276 and 278).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450363B2
Source datasetuspto-grants-2013_05
ORD IDord-2e7e3e148aca4ae9a54f369622779e32
Source noteuspto-grants-2013_05