| Identification | Back Directory | [Name]
N-(2-hydroxyethyl)acetoacetamide | [CAS]
24309-97-5 | [Synonyms]
Acetoacet-N-hydroxyethylamide
beta-(N-Acetoacetylamino)ethanol
N-(2-Hydroxyethyl)-3-oxobutanamide
N-(2-hydroxyethyl)-3-keto-butyramide | [EINECS(EC#)]
246-149-7 | [Molecular Formula]
C6H11NO3 | [MDL Number]
MFCD00066601 | [MOL File]
24309-97-5.mol | [Molecular Weight]
145.16 |
| Chemical Properties | Back Directory | [Appearance]
Yellow to brownisch solidifed melt | [Melting point ]
104-106 °C | [Boiling point ]
373.7±27.0 °C(Predicted) | [density ]
1.132±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [pka]
11.48±0.46(Predicted) |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow to brownisch solidifed melt | [Uses]
N-(2-Hydroxyethyl)acetoacetamide is used as intermediate for the syntheses of different organic chemicals, e.g. quinoxaline derivatives. Product Data Sheet | [Synthesis]
General procedure for the synthesis of N-(2-hydroxyethyl)-3-oxobutanamide from bis(vinylidene) ketone and 2-aminoethanol: 23 mL (0.38 mol) of 2-aminoethanol was added slowly and dropwise to 30 g (0.36 mol) of bis(vinylidene) ketone dissolved in 300 mL of tetrahydrofuran at -5 to 0 °C. The reaction mixture was stirred at 0 °C for 1 h. Complete consumption of the feedstock was confirmed by thin layer chromatography (TLC) monitoring. Subsequently, the solvent was removed by evaporation and the residue was purified by column chromatography. Finally, 41.44 g (0.29 mol, 80% yield) of the target compound was obtained as a white solid. The product was identified by infrared spectroscopy (IR, neat, cm?1) showing characteristic absorption peaks: 3273, 3097, 2973, 2938, 2880, 1710, 1646, 1558, 1494, 1465, 1420, 1362, 1347, 1312, 1297, 1215, 1190, 1166, 1052, 1038. (2H), 3.4 (4H), 2.2 (3H). | [References]
[1] Patent: US2013/109662, 2013, A1. Location in patent: Paragraph 0394; 0395; 0396; 0397; 0398; 0399
[2] Heterocycles, 1995, vol. 41, # 10, p. 2203 - 2220 |
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