Chemistry:Furfuryl alcohol

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Furfuryl alcohol[1]
Structural formula of furfuryl alcohol
Ball-and-stick model of the furfuryl alcohol molecule
Names
Preferred IUPAC name
(Furan-2-yl)methanol
Other names
Furan-2-ylmethanol
Furfuryl alcohol
2-Furanmethanol
2-Furancarbinol
2-(Hydroxymethyl)furan
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
UNII
Properties
C5H6O2
Molar mass 98.10 g/mol
Appearance colorless liquid
Odor burning odor[2]
Density 1.128 g/cm3
Melting point −29 °C (−20 °F; 244 K)
Boiling point 170 °C (338 °F; 443 K)
miscible
Hazards
Safety data sheet External MSDS
NFPA 704 (fire diamond)
Flammability code 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuelHealth code 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasReactivity code 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no codeNFPA 704 four-colored diamond
2
3
1
Flash point 65 °C; 149 °F; 338 K[2]
Explosive limits 1.8% - 16.3%[2]
Lethal dose or concentration (LD, LC):
397 ppm (mouse, 6 hr)
85 ppm (rat, 6 hr)
592 ppm (rat, 1 hr)[3]
597 ppm (mouse, 6 hr)[3]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 50 ppm (200 mg/m3)[2]
REL (Recommended)
 TWA 10 ppm (40 mg/m3) ST 15 ppm (60 mg/m3) [skin][2]
IDLH (Immediate danger)
 75 ppm[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Tracking categories (test):

Furfuryl alcohol is an organic compound containing a furan substituted with a hydroxymethyl group. It is a colorless liquid, but aged samples appear amber. It possesses a faint odor of burning and a bitter taste. It is miscible with but unstable in water. It is soluble in common organic solvents.[4]

Synthesis

Furfuryl alcohol is manufactured industrially by hydrogenation of furfural, which is itself typically produced from waste bio-mass such as corncobs or sugar cane bagasse. As such furfuryl alcohol may be considered a green chemical.[5] One-pot systems have been investigated to produce furfuryl alcohol directly from xylose using solid acid catalysts.[6]

Reactions

It undergoes many reactions including Diels–Alder additions to electrophilic alkenes and alkynes. Hydroxymethylation gives 1,5-bis(hydroxymethyl)furan. Hydrolysis gives levulinic acid. Upon treatment with acids, heat and/or catalysts, furfuryl alcohol can be made to polymerize into a resin, poly(furfuryl alcohol). Hydrogenation of furfuryl alcohol can proceed to give hydroxymethyl derivative of tetrahydrofuran and 1,5-pentanediol. The etherification reaction of furfuryl alcohol with alkyl or aryl halide (e.g. benzyl chloride) in the liquid-liquid-liquid triphase system with the help of a phase transfer catalyst also reported.[7] In the Achmatowicz reaction, also known as the Achmatowicz rearrangement, furfuryl alcohol is converted to a dihydropyran.

Applications

Resins, composites

The primary use of furfuryl alcohol is as a monomer for the synthesis of furan resins.[4][8] These polymers are used in thermoset polymer matrix composites, cements, adhesives, coatings and casting/foundry resins. Polymerization involves an acid-catalyzed polycondensation, usually giving a black cross-linked product.[9] A highly simplified representation is shown below.

Furan resin.svg

Because of its low molecular weight, furfuryl alcohol can impregnate the cells of wood, where it can be polymerized and bonded with the wood by heat, radiation, and/or catalysts or additional reactants. The treated wood (e.g. "Kebony") has improved moisture-dimensional stability, hardness, and decay and insect resistance; catalysts can include zinc chloride, citric, and formic acid, as well as borates.[10][11]

Use as rocket propellant (fuel component)

Furfuryl alcohol has been used in rocketry as a fuel which ignites hypergolically (immediately and energetically in contact) with white fuming nitric acid or red fuming nitric acid oxidizer.[12] The use of hypergolics avoids the need for an igniter. In late 2012, Spectra, a concept liquid rocket engine using white fuming nitric acid as the oxidizer to furfuryl alcohol fuel was static tested by Copenhagen Suborbitals.[13][14]

Safety

The median lethal dose for furfuryl alcohol ranges from 160 to 400 mg/kg (mouse or rabbit, oral).[citation needed]

See also

References

  1. ↑ Merck Index, 11th Edition, 4215.
  2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 NIOSH Pocket Guide to Chemical Hazards. "#0298". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0298.html. 
  3. ↑ 3.0 3.1 "Furfuryl alcohol". Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/idlh/98000.html. 
  4. ↑ 4.0 4.1 Hoydonckx, H. E.; Van Rhijn, W. M.; Van Rhijn, W.; De Vos, D. E.; Jacobs, P. A.. "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a12_119.pub2. 
  5. ↑ Mariscal, R.; Maireles-Torres, P.; Ojeda, M. et al. (2016). "Furfural: a Renewable and Versatile Platform Molecule for the Synthesis of Chemicals and Fuels". Energy Environ. Sci. 9 (4): 1144–1189. doi:10.1039/C5EE02666K. ISSN 1754-5692. https://digital.csic.es/bitstream/10261/184700/1/Mariscal_Furfural-A%20renewable_versatile_2016_postprint.pdf. 
  6. ↑ Gómez Millán, Gerardo; Sixta, Herbert (23 September 2020). "Towards the Green Synthesis of Furfuryl Alcohol in a One-Pot System from Xylose: a Review". Catalysts 10 (10): 1101. doi:10.3390/catal10101101. 
  7. ↑ Katole DO, Yadav GD. Process intensification and waste minimization using liquid-liquid-liquid triphase transfer catalysis for the synthesis of 2-((benzyloxy)methyl)furan. Molecular Catalysis 2019;466:112–21. https://doi.org/10.1016/j.mcat.2019.01.004
  8. ↑ Brydson, J. A. (1999). "Furan Resins". in J. A. Brydson. Plastics Materials (Seventh ed.). Oxford: Butterworth-Heinemann. pp. 810–813. doi:10.1016/B978-075064132-6/50069-3. ISBN 9780750641326. 
  9. ↑ Choura, Mekki; Belgacem, Naceur M.; Gandini, Alessandro (January 1996). "Acid-Catalyzed Polycondensation of Furfuryl Alcohol: Mechanisms of Chromophore Formation and Cross-Linking". Macromolecules 29 (11): 3839–3850. doi:10.1021/ma951522f. Bibcode: 1996MaMol..29.3839C. 
  10. ↑ Alfred J., Stamm (1977). "Chapter 9". Wood Technology: Chemical Aspects. ACS Symposium Series. 43. Washington: American Chemical Society. pp. 141–149. doi:10.1021/bk-1977-0043.ch009. ISBN 9780841203730. 
  11. ↑ Baysal, Ergun; Ozaki, S.Kiyoka; Yalinkilic, MustafaKemal (21 August 2004). "Dimensional stabilization of wood treated with furfuryl alcohol catalysed by borates". Wood Science and Technology. doi:10.1007/s00226-004-0248-2. 
  12. ↑ MUNJAL, N. L. (May 1970). "Ignition catalysts for furfuryl alcohol - Red fuming nitric acid bipropellant". AIAA Journal 8 (5): 980–981. doi:10.2514/3.5816. Bibcode: 1970AIAAJ...8..980M. 
  13. ↑ Madsen, Peter. "Spectra-testen" (in da). http://ing.dk/artikel/132056-spectra-testen. 
  14. ↑ Madsen, Peter. "Project SPECTRA: Experimental evaluation of a liquid storable propellant". Copenhagen Suborbitals. http://copenhagensuborbitals.com/public/spectra.pdf. 

External links



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