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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245247Generated: October 30, 2026

Benzoyl Peroxide → Methyl 3-(bromomethyl)-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

https://huagongshe.com/reaction/245247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-methyl-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylateHCID 67383507—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 3-(bromomethyl)-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylateHCID 67383823—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of methyl 3-methyl-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate (2.66 g, 6.28 mmol) in carbon tetrachloride (41.9 mL) was added N-bromosuccinimide (1.454 g, 8.17 mmol) and benzoyl peroxide (0.152 g, 0.628 mmol). The resulting mixture was heated at 100° C. for 18 h. The mixture was cooled to room temperature and concentrated in vacuo to afford methyl 3-(bromomethyl)-6-(methylsulfonyl)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658636B2
Source datasetuspto-grants-2014_02
ORD IDord-3993fd06d28246e7950ce5cf07f56448
Source noteuspto-grants-2014_02