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17168-45-5

17168-45-5 Structure

17168-45-5 Structure
IdentificationBack Directory
[Name]

(E)-3-(dimethylamino)-1-(furan-2-yl)prop-2-en-1-one
[CAS]

17168-45-5
[Synonyms]

2-Propen-1-one, 3-(dimethylamino)-1-(2-furanyl)-
(E)-3-(dimethylamino)-1-(furan-2-yl)prop-2-en-1-on
(E)-3-(dimethylamino)-1-(furan-2-yl)prop-2-en-1-one
[Molecular Formula]

C9H11NO2
[MDL Number]

MFCD00121186
[MOL File]

17168-45-5.mol
[Molecular Weight]

165.19
Chemical PropertiesBack Directory
[Melting point ]

92 °C(Solv: xylene (1330-20-7))
[Boiling point ]

231.8±36.0 °C(Predicted)
[density ]

1.071±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

6.42±0.70(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2932190090
Hazard InformationBack Directory
[Synthesis]

2-Acetylfuran

1192-62-7

N,N-Dimethylformamide dimethyl acetal

4637-24-5

(E)-3-(dimethylamino)-1-(furan-2-yl)prop-2-en-1-one

17168-45-5

General procedure: 2-acetylfuran (25.0 g, 0.227 mol) was mixed with N,N-dimethylformamide dimethyl acetal (40 mL) and the reaction was stirred at 100 °C for 9 hours. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated to remove the volatile components. Ether and hexane were added to the concentrated residue and the precipitated solid product was collected by filtration. The solid was washed with hexane to give the final 3-(dimethylamino)-1-(furan-2-yl)prop-2-en-1-one (36.5 g, 97% yield) as a brown solid. 3.4 Hz), 7.68 (1H, double peaks, J = 12.6 Hz), 7.79 (1H, double double heavy peaks, J = 0.8, 2.0 Hz).

[References]

[1] Patent: EP1439175, 2004, A1. Location in patent: Page 45-46
[2] Patent: US2004/6082, 2004, A1. Location in patent: Page/Page column 22
[3] Journal of Heterocyclic Chemistry, 1996, vol. 33, # 6, p. 1707 - 1710
[4] Organic Process Research and Development, 2008, vol. 12, # 3, p. 490 - 495
[5] Journal of the Korean Chemical Society, 2011, vol. 55, # 2, p. 243 - 250
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