Methylcyclopentane

Source: Wikipedia, the free encyclopedia.
Methylcyclopentane
Names
Preferred IUPAC name
Methylcyclopentane
Identifiers
3D model (
JSmol
)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard
100.002.277 Edit this at Wikidata
EC Number
  • 202-503-2
UNII
UN number 2298
  • InChI=1S/C6H12/c1-6-4-2-3-5-6/h6H,2-5H2,1H3
  • CC1CCCC1
Properties
C6H12
Molar mass 84.162 g·mol−1
Appearance Colorless liquid
Density 0.749 g/cm3[1]
Melting point −142.4 °C (−224.3 °F; 130.8 K)[1]
Boiling point 71.8 °C (161.2 °F; 344.9 K)[1]
Insoluble
-70.17·10−6 cm3/mol
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
flammable
Flash point −4 °C (25 °F; 269 K)
260 °C (500 °F; 533 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Methylcyclopentane is an

reformers to benzene.[2] The C6 core of methylcyclopentane is not perfectly planar and can pucker to alleviate stress in its structure.[3]

The conversion of methylcyclopentane to benzene is a classic aromatization reaction, specifically a dehydroisomerization. This platinum (Pt)-catalyzed process is practiced on scale in the production of gasoline from petroleum.

History

In 1895,

hydriodic acid. Prior to that, several chemists (such as Marcellin Berthelot in 1867,[4][5] and Adolf von Baeyer in 1870[6]) had tried and failed to synthesize cyclohexane
using this method.

References

  1. ^ .
  2. .
  3. .
  4. ^ Bertholet (1867). "Nouvelles applications des méthodes de réduction en chimie organique" [New applications of reduction methods in organic chemistry]. Bulletin de la Société Chimique de Paris (in French). series 2 (7): 53–65.
  5. ^ Bertholet (1868). "Méthode universelle pour réduire et saturer d'hydrogène les composés organiques" [Universal method for reducing and saturating organic compounds with hydrogen]. Bulletin de la Société Chimique de Paris (in French). series 2 (9): 8–31. En effet, la benzine, chauffée à 280° pendant 24 heures avec 80 fois son poids d'une solution aqueuse saturée à froid d'acide iodhydrique, se change à peu près entièrement en hydrure d'hexylène, C12H14, en fixant 4 fois son volume d'hydrogène: C12H6 + 4H2 = C12H14 … Le nouveau carbure formé par la benzine est un corps unique et défini: il bout à 69°, et offre toutes les propriétés et la composition de l'hydrure d'hexylène extrait des pétroles. [In effect, benzene, heated to 280° for 24 hours with 80 times its weight of an aqueous solution of cold saturated hydroiodic acid, is changed almost entirely into hydride of hexylene, C12H14, [Note: this formula for hexane (C6H14) is wrong because chemists at that time used the incorrect atomic mass for carbon.] by fixing [i.e., combining with] 4 times its volume of hydrogen: C12H6 + 4H2 = C12H14 The new carbon compound formed by benzene is a unique and well-defined substance: it boils at 69° and presents all the properties and the composition of hydride of hexylene extracted from oil.)]
  6. ^ Adolf Baeyer (1870). "Ueber die Reduction aromatischer Kohlenwasserstoffe durch Jodphosphonium" [On the reduction of aromatic compound by phosphonium iodide [H4IP]]. Annalen der Chemie und Pharmacie. 55: 266–281. Bei der Reduction mit Natriumamalgam oder Jodphosphonium addiren sich im höchsten Falle sechs Atome Wasserstoff, und es entstehen Abkömmlinge, die sich von einem Kohlenwasserstoff C6H12 ableiten. Dieser Kohlenwasserstoff ist aller Wahrscheinlichkeit nach ein geschlossener Ring, da seine Derivate, das Hexahydromesitylen und Hexahydromellithsäure, mit Leichtigkeit wieder in Benzolabkömmlinge übergeführt werden können. [During the reduction [of benzene] with sodium amalgam or phosphonium iodide, six atoms of hydrogen are added in the extreme case, and there arise derivatives, which derive from a hydrocarbon C6H12. This hydrocarbon is in all probability a closed ring, since its derivatives — hexahydromesitylene [1,3,5 - trimethyl cyclohexane] and hexahydromellithic acid [cyclohexane-1,2,3,4,5,6-hexacarboxylic acid] — can be converted with ease again into benzene derivatives.]