| 词条 | 2.2.2-Propellane |
| 释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 418039735 | Name=[2.2.2]Propellane | ImageFileL1 = 2.2.2-propellane.svg | ImageFileR1 = 2.2.2-propellane.png | ImageSizeR1 = 150px | IUPACName = Tricyclo[2.2.2.01,4]octane | OtherNames = |Section1={{Chembox Identifiers | CASNo = 36120-88-4 | CASNo_Ref = {{cascite|correct|??}} | PubChem = 564666 | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 490864 | SMILES = C1C23C(CC2)(CC3)C1 | InChI = 1/C8H12/c1-2-8-5-3-7(1,8)4-6-8/h1-6H2 | InChIKey = GPMHXZWOEIWUPW-UHFFFAOYAI | StdInChI_Ref = {{stdinchicite|changed|chemspider}} | StdInChI = 1S/C8H12/c1-2-8-5-3-7(1,8)4-6-8/h1-6H2 | StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | StdInChIKey = GPMHXZWOEIWUPW-UHFFFAOYSA-N}} |Section2={{Chembox Properties | C=8 | H=12 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }} [2.2.2]Propellane, formally tricyclo[2.2.2.01,4]octane is an organic compound, a member of the propellane family. It is a hydrocarbon with formula C8H12, or C2(C2H4)3. Its molecule has three rings with four carbon atoms each, sharing one C–C bond. This compound is unstable (although not as much as [1.1.1]propellane; however it is less persistent than [1.1.1]propellane[1]). The bond angles on the shared carbons are considerably strained: three of them are close to 90°, the other three to 120°. The strain energy is estimated to be 93 kcal/mol (390 kJ/mol). Synthesis[2.2.2]Propellane was first synthesized in 1973 by the group of Philip Eaton (who had earlier obtained cubane),[2] according to the following scheme: The synthesis begins with photochemical [2+2]cycloaddition of ethylene on the cyclohexene derivative 1 to produce the bicyclic compound 2, followed by elimination reaction with potassium t-butoxide of acetic acid to cyclobutene 3, followed by another cycloaddition with ethylene to 4. This compound is converted to the diazo ketone 5 by deprotonation (using acetic acid and sodium methoxide) and reaction with tosyl azide. The ketone then undergoes Wolff rearrangement to ketene 6. Ozonolysis forms the ketone 7, another diazotation yields the ketene 8, which undergoes Wolff rearrangement again to the ketene 9. Reaction with dimethylamine affords the [2.2.2]propellane backbone with a dimethylamide substituent 10. The final product 10 was found to spontaneously isomerize in solution to the monocyclic amide 11, with a half-life of 28 minutes at room temperature. DerivativesA highly fluorinated [2.2.0]propellane was also synthesized by the group of David Lemal.[3] See also
References1. ^{{Cite web|url=https://www.thieme.de/shop/Houben-Weyl--SoS/de-Meijere-Butenschoen-Chow-Fitjer-Haufe-Houben-Weyl-Methods-of-Organic-Chemistry-9783131819840/p/000000009583004404|title=Houben-Weyl Methods of Organic Chemistry Vol. E 17e, 4th Edition Supplement (E-Book PDF) - Thieme.de - Thieme Webshop - Armin de Meijere, Holger Butenschön, Hak-Fun Chow, Lutz Fitjer, Günter Haufe|website=Thieme Webshop|language=de|access-date=2017-10-21}} {{DEFAULTSORT:Propellane, 2.2.2}}2. ^{{cite journal|first1=Philip E.|last1=Eaton|first2=George H.|last2=Temme|authorlink=Philip Eaton|date=1973|title=[2.2.2]Propellane system|journal=J. Am. Chem. Soc.|volume=95|issue=22|pages=7508–7510|DOI=10.1021/ja00803a052}} 3. ^{{cite journal|last1=Zhang|first1=Y.|last2=Smith|first2=J.R.|last3=Lemal|first3=D.M.|date=1996|title=Octafluorobicyclo[2.2.0]hex-1(4)-ene: A Greatly Strained Alkene with Novel Reactivity|journal=J. Am. Chem. Soc.|volume=39|page=9454|doi=10.1021/ja961656o}} 3 : Cycloalkanes|Tricyclic compounds|Cyclobutanes |
| 随便看 |
|
开放百科全书收录14589846条英语、德语、日语等多语种百科知识，基本涵盖了大多数领域的百科知识，是一部内容自由、开放的电子版国际百科全书。