Phenylacetylene

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title: "Phenylacetylene" type: doc version: 1 created: 2026-02-28 author: "Wikipedia contributors" status: active scope: public tags: ["phenyl-compounds", "ethynyl-compounds", "c2-benzenes"] topic_path: "general/phenyl-compounds" source: "https://en.wikipedia.org/wiki/Phenylacetylene" license: "CC BY-SA 4.0" wikipedia_page_id: 0 wikipedia_revision_id: 0

|Watchedfields = changed |verifiedrevid = 464200987 |Name = Phenylacetylene |ImageFile = Phenylacetylene.svg |ImageName = Phenylacetylene |ImageFile1 = Phenylacetylene-3D-balls.png |PIN = Ethynylbenzene |OtherNames = Phenylacetylene |Section1={{Chembox Identifiers |ChemSpiderID_Ref = |ChemSpiderID = 10364 |PubChem = 10821 |InChI = 1/C8H6/c1-2-8-6-4-3-5-7-8/h1,3-7H |InChIKey = UEXCJVNBTNXOEH-UHFFFAOYAC |ChEMBL_Ref = |ChEMBL = 234833 |StdInChI_Ref = |StdInChI = 1S/C8H6/c1-2-8-6-4-3-5-7-8/h1,3-7H |StdInChIKey_Ref = |StdInChIKey = UEXCJVNBTNXOEH-UHFFFAOYSA-N |CASNo_Ref = |CASNo = 536-74-3 |UNII_Ref = |UNII = 239WSR2IBO |SMILES = C#Cc1ccccc1 |Section2={{Chembox Properties |Formula = C8H6 |MolarMass = 102.133 g/mol |Density = 0.93 g/cm3 |MeltingPtC = -45 |BoilingPtC = 142 to 144 |pKa = 28.7 (DMSO), 23.2 (aq, extrapolated) |MagSus = −72.01·10−6 cm3/mol

Phenylacetylene is an alkyne hydrocarbon containing a phenyl group. It exists as a colorless, viscous liquid. In research, it is sometimes used as an analog for acetylene; being a liquid, it is easier to handle than acetylene gas.

Preparation

In the laboratory, phenylacetylene can be prepared by elimination of hydrogen bromide from styrene dibromide using sodium amide in ammonia:

:[[File:Phenylacetylene prepn.png|350px]]

It can also be prepared by the elimination of hydrogen bromide from bromostyrene using molten potassium hydroxide. Yet another method involves the Sonogashira coupling of iodobenzene with trimethylsilylacetylene, followed by removal of the trimethylsilyl group using TBAF.

Reactions

Phenylacetylene is a prototypical terminal acetylene, undergoing many reactions expected of that functional group. It undergoes semihydrogenation over Lindlar catalyst to give styrene. In the presence of base and copper(II) salts, it undergoes oxidative coupling to give diphenylbutadiyne. In the presence of metal catalysts, it undergoes oligomerization, trimerization, and even polymerization. :[[Image:Cyclotri limits.png]]

In the presence of gold or mercury reagents, phenylacetylene hydrates to give acetophenone: :PhC2H + H2O → PhC(O)CH3

References

References

  1. Bordwell, F.G.. (1988). "Equilibrium acidities in dimethyl sulfoxide solution". Acc. Chem. Res..
  2. (1971). "Acidity of hydrocarbons. XXXV. Equilibrium acidities of phenylacetylene and ''tert''-butylacetylene in cyclohexylamine". J. Am. Chem. Soc..
  3. Kenneth N. Campbell, Barbara K. Campbell. (1950). "Phenylacetylene".
  4. John C. Hessler. (1922). "Phenylacetylene".
  5. (2007). "Trimethylsilylacetylene".
  6. (1965). "Diphenyldiacetylene". Organic Syntheses.
  7. (2005). "A simple cobalt catalyst system for the efficient and regioselective cyclotrimerisation of alkynes". [[Chemical Communications]].
  8. (2003). "Oligomerization and Polymerization of Alkynes Catalyzed by Rhodium(I) Pyrazolate Complexes". [[Journal of Molecular Catalysis A: Chemical]].

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phenyl-compoundsethynyl-compoundsc2-benzenes