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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3,5-bis(trifluoromethyl)benzene | HCID 67602 | — |
| Reactant | 4-chloro-2,6-dimethylquinoline | HCID 234275 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178506227 | HCID 178506227 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22721470 | HCID 22721470 | — |
| Product | HCID 178506227 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06730418B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-f0919f80027b40ec970c1f1b4439c43b |
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| Source note | uspto-grants-2004_05 |
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