Chemistry:9-Borabicyclo(3.3.1)nonane
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| Names | |
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| IUPAC name
9-Borabicyclo[3.3.1]nonane
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| Other names
Borabicyclononane
Banana borane | |
| Identifiers | |
3D model (JSmol)
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| Abbreviations | 9-BBN |
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PubChem CID
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| Properties | |
| C16H30B2 | |
| Molar mass | 244.04 g·mol−1 |
| Density | 0.894 g/cm3 |
| Melting point | 153 to 155 °C (307 to 311 °F; 426 to 428 K) |
| Reacts | |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Warning |
| H250, H260, H314 | |
| P210, P222, P223, P231+232, P260, P264, P280, P301+330+331, P302+334, P303+361+353, P304+340, P305+351+338, P310, P321, P335+334, P363, P370+378, P402+404, P405, P422, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
9-Borabicyclo[3.3.1]nonane or 9-BBN is an organoborane compound. This colourless solid is used in organic chemistry as a hydroboration reagent. The compound exists as a hydride-bridged dimer, which easily cleaves in the presence of reducible substrates.[1] 9-BBN is also known by its nickname 'banana borane'.[2] This is because rather than drawing out the full structure, chemists often simply draw a banana shape with the bridging boron.[3][better source needed]
Preparation
9-BBN is prepared by the reaction of 1,5-cyclooctadiene and borane usually in ethereal solvents, for example:[4][5]
The compound is commercially available as a solution in tetrahydrofuran and as a solid. 9-BBN is especially useful in Suzuki reactions.[6][7][8]
Its highly regioselective addition on alkenes allows the preparation of terminal alcohols by subsequent oxidative cleavage with H2O2 in aqueous KOH. The steric demand of 9-BBN greatly suppresses the formation of the 2-substituted isomer compared to the use of borane.
See also
References
- ↑ Brown, H. C. (1975). Organic Syntheses via Boranes. New York: John Wiley & Sons. ISBN 0-471-11280-1. https://archive.org/details/organicsyntheses0000brow.
- ↑ Stix, Gary. "The Straight Dope: A Q&A with the Prof behind the Good Science in Breaking Bad" (in en). Nature America, Inc.. https://blogs.scientificamerican.com/talking-back/the-straight-dope-a-qa-with-the-prof-behind-the-good-science-in-breaking-bad/.
- ↑ "Molecules with Silly or Unusual Names - page 3". 2014-05-07. http://www.chm.bris.ac.uk/sillymolecules/sillymols3.htm.
- ↑ Soderquist, John A.; Brown, Herbert C. (1981). "Simple, remarkably efficient route to high purity, crystalline 9-borabicyclo[3.3.1]nonane (9-BBN) dimer". J. Org. Chem. 46 (22): 4599–4600. doi:10.1021/jo00335a067.
- ↑ Soderquist, John A.; Alvin, Negron (1982). "9-Borabicyclo[3.3.1]nonane Dimer". Organic Syntheses 70: 169. doi:10.15227/orgsyn.070.0169.
- ↑ Ishiyama, Tatsuo; Miyaura, Norio; Suzuki, Akira. "Palladium(0)-catalyzed reaction of 9-alkyl-9-borabicyclo[3.3.1nonane with 1-bromo-1-phenylthioethene: 4-(3-cyclohexenyl)-2-phenylthio-1-butene"]. Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv9p0107.; Collective Volume, 9, pp. 107
- ↑ Balog, A.; Meng, D.; Kamenecka, T.; Bertinato, P.; Su, D.-S.; Sorensen, E. J.; Danishefsky, S. J. (1996). "Total Synthesis of (−)-Epothilone A". Angew. Chem. Int. Ed. Engl. 35 (2324): 2801. doi:10.1002/anie.199628011.
- ↑ Liu, J.; Lotesta, S. D.; Sorensen, E. J. (2011). "A concise synthesis of the molecular framework of pleuromutilin". Chem. Commun. 47 (5): 1500–1502. doi:10.1039/C0CC04077K. PMID 21079876.
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