Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581455Generated: November 2, 2026

1-Bromo-3,5-bis(trifluoromethyl)benzene → HCID 22721470, compound

https://huagongshe.com/reaction/1581455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3,5-bis(trifluoromethyl)benzeneHCID 67602—
Reactant4-chloro-2,6-dimethylquinolineHCID 234275—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178506227HCID 178506227—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22721470HCID 22721470—
ProductHCID 178506227HCID 178506227—

Reaction Steps

Magnesium (1.60 g) was added to THF (60 ml) in a nitrogen atmosphere and 3,5-bis (trifluoromethyl)phenylbromide (17.58 g) was dropped. The resulting mixture was stirred for 30 minutes at room temperature and a THF solution of 3,5-bis (trifluoromethyl)phenylmagnesiumbromide was prepared. In a nitrogen atmosphere, 4-chloro-2,6-dimethylquinoline (2.88 g) and Ni(dpp)Cl2 (500 mg) were added to THF (30 ml) and dispersed. The THF solution of 3,5-bis(trifluoromethyl)phenylmagnesiumbromide prepared as above was dropped to the suspension and the resulting solution was stirred for 4 days at room temperature. Water was poured into the reaction solution, impurities were filtered, and extraction was performed using AcOEt (ethyl acetate). A drying process was applied using Na2SO4 and the solvent was removed under a reduced pressure. The residue was purified through a silica gel column (hexane/ethyl acetate=3/2) to obtain 4-(3,5-bis(trifluoromethyl)phenyl)-2,6-dimethylquinoline (4.40 g) represented by the following chemical formula (49).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730418B2
Source datasetuspto-grants-2004_05
ORD IDord-f0919f80027b40ec970c1f1b4439c43b
Source noteuspto-grants-2004_05