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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499593Generated: October 30, 2026

Ammonium formate → tert-Butyl 3-(pyridin-4-yl)propanoate

https://huagongshe.com/reaction/499593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactanttert-Butyl (E)-3-(4-Pyridyl)acrylateHCID 11805847—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Producttert-Butyl 3-(pyridin-4-yl)propanoateHCID 1479955965.1%

Reaction Steps

tert-Butyl (E)-3-(4-Pyridyl)acrylate (0.88 g, 4.3 mmol) was dissolved in ethanol (10 ml), and 10% palladium-carbon (0.17 g) and a solution of ammonium formate (1.4 g, 21.4 mmol) in water (2.5 ml) were added thereto. The reaction mixture was refluxed for 3 hrs. Palladium-carbon was filtered off. The reaction mixture was combined with water, concentrated under reduced pressure to the half amount and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated, and the residue was subjected to a silica gel (20 g) column chromatography. The fractions eluted with hexane-ethyl acetate (3:1, v/v) were collected and concentrated to give the titled compound (0.58 g, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767665B2
Source datasetuspto-grants-2010_08
ORD IDord-c2a1a25b24ee42b7a1dfc7409a1c1c03
Source noteuspto-grants-2010_08