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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509940Generated: November 4, 2026

Trifluoroacetic acid → HCID 29553240, compound

https://huagongshe.com/reaction/509940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantTriethylsilaneHCID 12052—
Reactanto-FluorobenzaldehydeHCID 67970—
Reactant2-Amino-5-bromopyridineHCID 70622—
SolventAcetonitrileHCID 6342—
ProductHCID 29553240HCID 2955324076%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096593B2
Source datasetuspto-grants-2015_08
ORD IDord-ed72b866d8ff418e8a639feb8428dbd2
Source noteuspto-grants-2015_08