HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509940Generated: November 4, 2026
Trifluoroacetic acid → HCID 29553240, compound
https://huagongshe.com/reaction/509940
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 29553240 | HCID 29553240 | 76% |
Reaction Steps
In a round bottom flask, 5-bromo-pyridin-2-ylamine (38, 4.05 g g, 23.4 mmol) was combined with 70.0 mL of acetonitrile, 2-fluoro-benzaldehyde (39, 2.45 mL, 23.4 mmol), triethylsilane (20.0 mL, 125 mmol) and trifluoroacetic acid (10.0 mL, 130 mmol). The reaction was stirred at 80° C. for 3 hours. The reaction was poured into aqueous potassium carbonate and extracted with ethyl acetate. The organic layer was dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography eluting with 20-60% ethyl acetate in hexane. Appropriate fractions were combined and the solvents removed under vacuum to provide the desired compound (40, 5.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096593B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-ed72b866d8ff418e8a639feb8428dbd2 |
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| Source note | uspto-grants-2015_08 |
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