Basic information Safety Supplier Related

5-HYDROXY-4-METHYL-2(5H)FURANONE

Basic information Safety Supplier Related

5-HYDROXY-4-METHYL-2(5H)FURANONE Basic information

Product Name:
5-HYDROXY-4-METHYL-2(5H)FURANONE
Synonyms:
  • (R,S)-5-Hydroxy-4-methyl-5H-furan-2-one
  • 4-Methyl-5-hydroxy-2(5H)-furanone
  • 5-HYDROXY-4-METHYL-2(5H)FURANONE
  • 2(5H)-FURANONE, 5-HYDROXY-4-METHYL
  • 5-HYDROXY-4-METHYL-5H-FURAN-2-ONE
  • 5-Hydroxy-4-Methyl-2(5H)-Furan
  • 5-HYDROXYDODECANOIC LACTONE
  • 2(5H)-FURANONE, 5-HYDROXY-4-METHYL (INTERMEDIATES OF ISOTRETINOIN)
CAS:
40834-42-2
MF:
C5H6O3
MW:
114.1
EINECS:
609-869-6
Product Categories:
  • Intermediates of Isotretinoin
Mol File:
40834-42-2.mol
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5-HYDROXY-4-METHYL-2(5H)FURANONE Chemical Properties

Boiling point:
113 °C(Press: 0.05 Torr)
Density 
1.349±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO, Methanol (Slightly)
form 
Yellow to Dark Yellow
pka
10.04±0.40(Predicted)
Appearance
Light brown to brown Solid
InChI
InChI=1S/C5H6O3/c1-3-2-4(6)8-5(3)7/h2,5,7H,1H3
InChIKey
XRNPHZPFAWLRNJ-UHFFFAOYSA-N
SMILES
O1C(O)C(C)=CC1=O
CAS DataBase Reference
40834-42-2(CAS DataBase Reference)
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Safety Information

HS Code 
2932190090
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5-HYDROXY-4-METHYL-2(5H)FURANONE Usage And Synthesis

Chemical Properties

Brownish Yellow Semi Solid

Uses

5-Hydroxy-4-methyl-2(5H)-furanone is a non-halogenated furanone used in studies to verify the mutagenicity of halogen substituted furanones.

Synthesis

616-02-4

931-23-7

40834-42-2

Under nitrogen protection, 5.34 g (21.00 mmol) LiAlH(t-BuO)3 was dissolved in 40 cm3 anhydrous THF and added dropwise to a solution of 1.68 g (15.00 mmol) citraconic anhydride dissolved in 50 cm3 anhydrous THF over a period of 30 min, and the reaction temperature was maintained at -30 °C. After the dropwise addition was completed, the temperature of the reaction system was raised to -15°C and maintained for 3 hours. Subsequently, the reaction mixture was slowly warmed up to room temperature. Upon completion of the reaction, the reaction was quenched with 50 cm3 1M HCl solution, followed by washing with saturated NaCl solution and extraction of the crude product with EtOAc (3 x 50 cm3). The organic phases were combined and dried with MgSO? The solvent was removed by concentration under reduced pressure to give the crude product. Purification by silica gel column chromatography (eluent: petroleum ether/ethyl acetate=80:20) afforded 5-hydroxy-3-methylfuran-2(5H)-one (7a, 1.023 g, 60% yield) and 4-methyl-5-hydroxyfuran-2-one (7b, 116 mg, 7% yield) as yellow oils, respectively.TLC analysis (unfolding agent: petroleum ether/ethyl acetate= 80:20) showed that the Rf values of 7a and 7b were 0.16 and 0.15, respectively. 1H NMR (400 MHz, acetone-d6) δ of 7a: 6.67 (bs, 1H), 6.02 (bs, 1H), 5.87 (p, J = 1.5 Hz, 1H), 2.08 (d, J = 1.5 Hz, 3H) ppm; 13C NMR (100 MHz, acetone-d6) ppm. MHz, acetone-d6) δ: 171.30 (C), 166.65 (C), 118.68 (CH), 100.25 (CH), 13.15 (CH3) ppm; MS (EI): m/z (%) = 114.0 ([M]+, 2), 113.0 (7), 86.0 (61), 85.0 (13), 69.0 ( 100), 68.0 (82), 41.1 (50), 40.1 (65), 39.1 (93).

References

[1] Monatshefte fur Chemie, 2018, vol. 149, # 8, p. 1475 - 1480

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