HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926458Generated: October 27, 2026
Toluene → 6-Bromo-4-chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinoline
https://huagongshe.com/reaction/926458
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 6-Bromo-2,4-dichloro-3-(4-(trifluoromethyl)benzyl)quinoline | HCID 86715628 | — |
| Solvent | Methylenechloride Hexane | HCID 21226440 | — |
| Product | 6-Bromo-4-chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinoline | HCID 86715627 | — |
Reaction Steps
To a 1 L flask containing 6-bromo-2,4-dichloro-3-(4-(trifluoromethyl)benzyl)quinoline (32.5 g, 74.7 mmol, Intermediate 12: step c) was added toluene (550 mL) followed by solid sodium methoxide (40 g, 740 mmol, 97% purity) at room temperature. The suspension was stirred at reflux (˜118° C.) in an aluminum mantle. TLC (50% hexane-DCM) and HPLC after 5.5 hours showed the reaction to be complete. The reaction mixture was filtered through Celite® while still warm (˜80° C.) and rinsed with warm toluene (˜70° C., 500 mL). The colorless filtrate was concentrated and the resulting residue solidified to provide the title compound as an off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284308B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-77555f90f47d46629c970f24381e9f8c |
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| Source note | uspto-grants-2016_03 |
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