HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778272Generated: November 2, 2026
Trifluoroacetic acid → HCID 118324072, compound
https://huagongshe.com/reaction/1778272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 118324107 | HCID 118324107 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118324072 | HCID 118324072 | — |
Reaction Steps
Into a 500-mL 3-necked round-bottom flask, was placed (4-bromo-8-methoxyquinolin-6-yl)bis(4-chlorophenyl)methanol (6 g, 12.27 mmol, 1.00 equip), dichloromethane (200 mL), triethylsilane (8 mL), and trifluoroacetic acid (24 mL). The resulting solution was stirred overnight at 25° C. The resulting solution was diluted with DCM (100 mL). The resulting mixture was washed with saturated sodium bicarbonate (3×100 mL) and dried over anhydrous sodium sulfate. The solids were filtered out. The residue was applied onto a silica gel column with ethyl acetate:petroleum ether (1:1) to yield 6-[bis(4-chlorophenyl)methyl]-4-bromo-8-methoxyquinoline as a yellow solid. LCMS (ES, m/z) 474 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266835B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-cee5178860a04e20b3719828f9b9fc6c |
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| Source note | uspto-grants-2016_02 |
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