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 |
| ChemSpider | |
| ECHA InfoCard | 100.005.456 |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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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 labelling: | |
 
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| Warning | |
| H250, H260, H314 | |
| P210, P222, P223, P231 P232, P260, P264, P280, P301 P330 P331, P302 P334, P303 P361 P353, P304 P340, P305 P351 P338, P310, P321, P335 P334, P363, P370 P378, P402 P404, P405, P422, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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
[edit]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
[edit]References
[edit]- ^ Brown, H. C. (1975). Organic Syntheses via Boranes. New York: John Wiley & Sons. ISBN 0-471-11280-1.
- ^ Stix, Gary. "The Straight Dope: A Q&A with the Prof behind the Good Science in Breaking Bad". Scientific American Blog Network. Nature America, Inc. Retrieved 18 June 2017.
- ^ Yale (2016-03-14). "Yale educational material: Hydroboration". Hydroboration Mechanics. Archived from the original on 13 August 2024.
- ^ 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/jo00335a067.4599-4600&rft.date=1981&rft_id=info:doi/10.1021/jo00335a067&rft.aulast=Soderquist&rft.aufirst=John A.&rft.au=Brown, Herbert C.&rfr_id=info:sid/en.wikipedia.org:9-Borabicyclo(3.3.1)nonane" class="Z3988">
- ^ 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[3.3.1]nonane with 1-bromo-1-phenylthioethene: 4-(3-cyclohexenyl)-2-phenylthio-1-butene". Organic Syntheses; Collected Volumes, vol. 9, p. 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. PMC 3156455. PMID 21079876.1500-1502&rft.date=2011&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156455#id-name=PMC&rft_id=info:pmid/21079876&rft_id=info:doi/10.1039/C0CC04077K&rft.aulast=Liu&rft.aufirst=J.&rft.au=Lotesta, S. D.&rft.au=Sorensen, E. J.&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156455&rfr_id=info:sid/en.wikipedia.org:9-Borabicyclo(3.3.1)nonane" class="Z3988">