Furan

Template:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox HazardsTemplate:Chembox headerbarTemplate:Chembox headerbarTemplate:Chembox PointGroupTemplate:Chembox Datapage checkTemplate:Yesno

Furan

Template:Chembox image sbs cell
Template:Chembox image sbs cell
Template:Longitem	Template:Unbulleted list
Template:Longitem	103221
ChEBI	Template:Unbulleted list
ChemSpider	Template:Unbulleted list
DrugBank	Template:Unbulleted list
EC Number	Template:Unbulleted list
Template:Longitem	25716
KEGG	Template:Unbulleted list
Template:Longitem	Template:Unbulleted list
RTECS number	Template:Unbulleted list
UN number	2389
Template:Longitem	Template:Chembox Elements/molecular formula
Molar mass	Template:Chem molar mass
Appearance	Colorless, volatile liquid
Density	0.936 g/mL
Melting point	Template:Chembox CalcTemperatures
Boiling point	Template:Chembox CalcTemperatures
Template:Longitem	−43.09·10−6 cm3/mol
Template:Longitem	Pyrrole Thiophene
Template:Longitem	Tetrahydrofuran (THF) 2,5-Dimethylfuran Benzofuran Dibenzofuran

Furan is a heterocyclic organic compound, consisting of a five-membered aromatic ring with four carbon atoms and one oxygen atom. Chemical compounds containing such rings are also referred to as furans.

Furan is a colorless, flammable, highly volatile liquid with a boiling point close to room temperature. It is soluble in common organic solvents, including alcohol, ether, and acetone, and is slightly soluble in water. Its odor is strong and chloroform-like. It is toxic and may be carcinogenic in humans. Furan is used as a starting point for other speciality chemicals.

History

The name "furan" comes from the Latin furfur, which means bran (furfural is produced from bran). The first furan derivative to be described was 2-furoic acid, by Carl Wilhelm Scheele in 1780. Another important derivative, furfural, was reported by Johann Wolfgang Döbereiner in 1831 and characterised nine years later by John Stenhouse. Furan itself was first prepared by Heinrich Limpricht in 1870, although he called it "tetraphenol" (as if it were a four-carbon analog to phenol, C₆H₅OH).

Production

Industrially, furan is manufactured by the palladium-catalyzed decarbonylation of furfural, or by the copper-catalyzed oxidation of 1,3-butadiene:

File:Manufacture of furan.png

In the laboratory, furan can be obtained from furfural by oxidation to 2-furoic acid, followed by decarboxylation. It can also be prepared directly by thermal decomposition of pentose-containing materials, and cellulosic solids, especially pine wood.

Synthesis of furans

The Feist–Benary synthesis is a classic way to synthesize furans. The reaction involves alkylation of 1,3-diketones with α-bromoketones followed by dehydration of an intermediate hydroxydihydrofuran. The other traditional route involve the reaction of 1,4-diketones with phosphorus pentoxide (P₂O₅) in the Paal–Knorr synthesis.

Many routes exist for the synthesis of substituted furans.

• Furan in nature and commerce
• The drug ranitidine, also known as Zantac.
  The drug ranitidine, also known as Zantac.
• Rosefuran, an aroma compound found in rose oil.[10]
  Rosefuran, an aroma compound found in rose oil.
• Furfural, derived from sugars, is the major source of furans.
  Furfural, derived from sugars, is the major source of furans.
• Methanofuran is a cofactor in methanogenesis.
  Methanofuran is a cofactor in methanogenesis.

Structure and bonding

Furan has aromatic character because one of the lone pairs of electrons on the oxygen atom is delocalized into the ring, creating a 4n + 2 aromatic system (see Hückel's rule). The aromaticity is modest relative to that for benzene and related heterocycles thiophene and pyrrole. The resonance energies of benzene, pyrrole, thiophene, and furan are, respectively, Template:Cvt. Thus, these heterocycles, especially furan, are far less aromatic than benzene, as is manifested in the lability of these rings. The molecule is flat but the C=C groups attached to oxygen retain significant double bond character. The other lone pair of electrons of the oxygen atom extends in the plane of the flat ring system.

Examination of the resonance contributors shows the increased electron density of the ring relative to benzene, leading to increased rates of electrophilic substitution.

Resonance contributors of furan

Reactivity

Because of its partial aromatic character, furan's behavior is intermediate between that of an enol ether and an aromatic ring. It is dissimilar vs ethers such as tetrahydrofuran.

Like enol ethers, 2,5-disubstituted furans are susceptible to hydrolysis to reversibly give 1,4-diketones.

Furan serves as a diene in Diels–Alder reactions with electron-deficient dienophiles such as ethyl (E)-3-nitroacrylate. The reaction product is a mixture of isomers with preference for the endo isomer:

Furan Diels–Alder reaction with ethyl (E)-3-nitroacrylate

Diels-Alder reaction of furan with arynes provides corresponding derivatives of dihydronaphthalenes, which are useful intermediates in synthesis of other polycyclic aromatic compounds.

Reaction of furan with a benzyne

• It is considerably more reactive than benzene in electrophilic substitution reactions, due to the electron-donating effects of the oxygen heteroatom. It reacts with bromine at 0 °C to give 2-bromofuran.

• Hydrogenation of furans sequentially affords dihydrofurans and tetrahydrofurans.
• In the Achmatowicz reaction, furans are converted to dihydropyran compounds.
• Pyrrole can be prepared industrially by treating furan with ammonia in the presence of solid acid catalysts, such as SiO₂ and Al₂O₃.

Safety

Furan is found in heat-treated commercial foods and is produced through thermal degradation of natural food constituents. It can be found in roasted coffee, instant coffee, and processed baby foods. Research has indicated that coffee made in espresso makers and coffee made from capsules contain more furan than that made in traditional drip coffee makers, although the levels are still within safe health limits.

Exposure to furan at doses about 2,000 times the projected level of human exposure from foods increases the risk of hepatocellular tumors in rats and mice and bile duct tumors in rats. Furan is therefore listed as a possible human carcinogen.

See also

• BS 4994 – Furan resin as thermoset FRP for chemical process plant equipments
• Furanocoumarin
• Furanoflavonoid
• Furanose
• Furantetracarboxylic acid
• Simple aromatic rings
• Furan fatty acids
• Tetrahydrofuran

External links

• Recent synthetic methods