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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734902Generated: October 29, 2026

Allyl Alcohol → 3-(6-Isopropylaminopyridin-3-yl)propionaldehyde

https://huagongshe.com/reaction/734902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantSodium BicarbonateHCID 516892—
Reactant5-iodo-N-isopropylpyridin-2-amineHCID 69058026—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-(6-Isopropylaminopyridin-3-yl)propionaldehydeHCID 86076995—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 1.80 g (6.87 mmol) of (5-iodopyridin-2-yl)isopropylamine, 1.40 mL (10.7 mmol) of prop-2-en-1-ol, 1.39 g (16.49 mmol) of sodium hydrogen carbonate, 1.72 g (6.18 mmol) of tetrabutylammonium chloride, and 46 mg (0.20 mmol) of palladium (II) acetate in 10 mL of DMF was stirred under argon for 20 hours at 50° C. The reaction mixture was diluted with water and EtOAc, the organic phase was separated off, washed several times with water, and dried over magnesium sulfate. After the desiccant and solvent had been eliminated, the residue was purified by chromatography (silica gel, PE/EtOAc 1:1). Yield: 300 mg (23% of theoretical); ClIH16N2O (M=192.258); calc.: molpeak (M+H)+:193; found: molpeak (M+H)+:193; HPLC-MS: 3.58 minutes (method G).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592358B2
Source datasetuspto-grants-2009_09
ORD IDord-4aefb381620f4cb9a07ccf2d2d9b5b7b
Source noteuspto-grants-2009_09