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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356749Generated: October 29, 2026

Formic Acid → HCID 86593203, compound

https://huagongshe.com/reaction/2356749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67548065HCID 67548065—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 86593203HCID 86593203—

Reaction Conditions

Temperature50 °C

Reaction Steps

To acetic anhydride (2.39 ml) was added dropwise formic acid (0.97 ml) under ice-cooling, and the mixture was stirred at 50° C. for 30 minutes. The mixture was ice-cooled again, and diluted with tetrahydrofuran (9 ml). To the mixture were added 2-amino-1-(3-pyridyl)-1-butanone dihydrochloride (600 mg) and triethylamine (1.41 ml), and the mixture was stirred under ice-cooling for 1.5 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. The resulting residue was triturated with ethyl acetate-diethyl ether to obtain 2-formylamino-1-(3-pyridyl)-1-butanone (440 mg) as colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759373B2
Source datasetuspto-grants-2010_07
ORD IDord-ab6077cd3c624db296ad87e0ee0d9856
Source noteuspto-grants-2010_07