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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54161Generated: October 25, 2026

Beta-Alanine → DNP-beta-alanine

https://huagongshe.com/reaction/54161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBeta-AlanineHCID 239—
ReactantDinitrofluorobenzeneHCID 6264—
SolventEthanolHCID 702—
SolventSodium BicarbonateHCID 516892—
ProductDNP-beta-alanineHCID 410085177%

Reaction Steps

To a solution of beta-alanine (1.0 g, 11.1 mmole) in 50 ml of 1M NaHCO3 was added 2,4-dinitrofluorobenzene (10.4 g, 56 mmole) in 100 ml of ethanol. The reaction mixture was stirred at room temperature for 2 hours and evaporated to remove the volatile in vacuo. The residue was transferred to a separatory funnel with water and washed twice with ethyl ether. The aqueous layer was acidified with 1N HCl until precipitation was complete. The mixture was filtered and the wet cake washed with ether. This purification process, starting from dissolving the solid in 1M NaHCO3, washing the ether, and precipitating with 1N HCl, was repeated in the same manner to give yellow solid (1.6 g, 77%). e(MeOH)=7900 (260 nm), 15900 (350 nm). NMR spectral analysis was consistent with the structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622825
Source datasetuspto-grants-1997_04
ORD IDord-caecbc10b9424b439d826648242cfab7
Source noteuspto-grants-1997_04