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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038655Generated: October 26, 2026

Trifluoroacetic acid → 4-(4-Bromo-pyridin-2-yl)-4-oxo-butyraldehyde

https://huagongshe.com/reaction/1038655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58191758HCID 58191758—
SolventDichloromethaneHCID 6344—
Product4-(4-Bromo-pyridin-2-yl)-4-oxo-butyraldehydeHCID 58191780—

Reaction Steps

To a solution of 1-(4-bromo-pyridin-2-yl)-4,4-dimethoxy-butan-1-one (2) (crude from Step 2, 11 g, 38.2 mmol) in 100 of CH2Cl2 at room temperature is added trifluoroacetic acid (10.9 g, 95.4 mmol) and the reaction mixture is stirred overnight. The reaction is concentrated, the residue dissolved in ethyl acetate (150 mL) and washed with water 3 times. The organic layers are combined, dried over Na2SO4 and the solvent evaporated. The residue is purified by flash column chromatography (30% EtOAc in hexanes) to give 4-(4-bromo-pyridin-2-yl)-4-oxo-butyraldehyde (3) as an yellow oil. (4.16 g, 45%): MS ES+244.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552003B2
Source datasetuspto-grants-2013_10
ORD IDord-d694091139344122a196e4acdbfc6cda
Source noteuspto-grants-2013_10