Basic information Safety Supplier Related

4-(Bromomethyl)-5-hydrofuran-2-one

Basic information Safety Supplier Related

4-(Bromomethyl)-5-hydrofuran-2-one Basic information

Product Name:
4-(Bromomethyl)-5-hydrofuran-2-one
Synonyms:
  • 4-(Bromomethyl)-5-hydrofuran-2-one
  • 4-(BroMoMethyl)furan-2(5H)-one
  • 3-(Bromomethyl)-2-buten-4-olide
  • 4-(Bromomethyl)-2(5H)-furanone
  • 4-(Bromomethyl)-2,5-dihydrofuran-2-one
  • 2(5H)-Furanone, 4-(bromomethyl)-
  • 4-Bromomethyl-5H-furan-2-one
  • 4-(Bromomethyl)-2,5-dihydrofuran-2-one - [B31582]
CAS:
61934-55-2
MF:
C5H5BrO2
MW:
177
Product Categories:
  • Heterocycles
Mol File:
61934-55-2.mol
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4-(Bromomethyl)-5-hydrofuran-2-one Chemical Properties

storage temp. 
Sealed in dry,Store in freezer, under -20°C
form 
liquid
color 
Yellow
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Safety Information

HS Code 
2932190090
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4-(Bromomethyl)-5-hydrofuran-2-one Usage And Synthesis

Synthesis

75887-43-3

61934-55-2

Synthesis of 4-(bromomethyl)furan-2(5H)-one (8): 5% aqueous sodium hydroxide solution (100 mL) was stirred with compound 7 (1.98 g, 7.68 mmol) at room temperature overnight. After completion of the reaction, the reaction mixture was extracted with dichloromethane (3 x 150 mL), the organic phase was washed sequentially with saturated aqueous sodium bicarbonate solution and distilled water, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification by column chromatography (eluent ratio 4:1 hexane:ethyl acetate) afforded the target product 8 as a mixture of enol-keto interconverting isomers in the form of a yellow oil (150 mg, 11% yield). Thin layer chromatography (TLC) showed an Rf value of 0.00 (eluent ratio 4:1 hexane:ethyl acetate). The NMR hydrogen spectra (500 MHz, CDCl3) δH of the ketone interconversion isomers: 4.24 (2H, single peak, CH2Br), 4.98 (2H, single peak, CH2), 6.16 (1H, single peak, CH). NMR carbon spectrum (125.77 MHz, CDCl3) δC: 41.33 (CH2Br), 74.05 (CH2), 121.09 (CH), 155.42 (C), 178.32 (C=O). NMR hydrogen spectrum (500 MHz, CDCl3) δH of the enol intercalation isomers: 2.30 (1H, multiple peaks, CH2CH), 4.20 (2H, multiple peaks, CH2Br), 4.74 (2H, multiple peaks, CH2), 6.09 (1H, single peaks, CH), 9.10 (1H, broad single peaks, OH). Mass spectra (EI): m/z 149 [M-CO]- (100%), 96 (40), 68 (50), 39 (70). Gas Chromatography (GC) retention time: 6.57 min.

References

[1] Journal of Mass Spectrometry, 2009, vol. 44, # 12, p. 1733 - 1741
[2] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 10, p. 3074 - 3077
[3] Tetrahedron, 1996, vol. 52, # 37, p. 12137 - 12158
[4] Bioorganic and Medicinal Chemistry, 2010, vol. 18, # 4, p. 1626 - 1632
[5] European Journal of Organic Chemistry, 2014, vol. 2014, # 19, p. 4053 - 4069

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