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| 化学名: | 9-ボラビシクロ[3.3.1]ノナン | | 英語化学名: | 9-Borabicyclo[3.3.1]nonane | | 别名: | 9-BORABICYCLO(3.3.1)NONANE SOLUTION, ~0. 5 M IN THF;9-Borabicyclo[3.3.1]nonane, 0.5M solution in THF;9-BBN,9-BORABICYCLO[3.3.1]NONANE;9-BORABICYCLO[3.3.1]NONANE (9BBN);9-BBN(0.5M in toluene);9-Borabicyclo[3.3.1]nonane0.5M solution in THFAcroSeal§3;1,5-(Boranediyl)cyclooctane;9-Borabicyclo[3.3.1]nonane, 0.5M solution inHexane | | CAS番号: | 280-64-8 | | 分子式: | C8H15B | | 分子量: | 122.02 | | EINECS: | 206-000-9 | | カテゴリ情報: | | | Mol File: | 280-64-8.mol | ![9-ボラビシクロ[3.3.1]ノナン](CAS/GIF/280-64-8.gif) |
| 融点 | 140-142 °C | | 沸点 | 68-70 °C | | 比重(密度) | 0.894 g/mL at 25 °C | | 闪点 | 1 °F | | 貯蔵温度 | Flammables area | | 溶解性 | Miscible with ether, hexane, benzene, toluene, carbon tetrachloride, chloroform, dimethylsulfide and dichloromethane. Slightly miscible with cyclohexane, dimethoxyethane, diglyme and dioxane. | | 水溶解度 | reacts | | Sensitive | Air & Moisture Sensitive | | BRN | 605509 | | 暴露限界値 | ACGIH: TWA 50 ppm; STEL 100 ppm (Skin)
OSHA: TWA 200 ppm(590 mg/m3)
NIOSH: IDLH 2000 ppm; TWA 200 ppm(590 mg/m3); STEL 250 ppm(735 mg/m3) | | InChIKey | FEJUGLKDZJDVFY-OCAPTIKFSA-N | | EPAの化学物質情報 | 9-Borabicyclo[3.3.1]nonane (280-64-8) |
| | 9-ボラビシクロ[3.3.1]ノナン Usage And Synthesis |
| 用途 | 9-BBN とは、有機合成化学において用いられる試剤のひとつ。ボランの誘導体としてアルケンのヒドロホウ素化反応に用いられる。一般に「ナインビービーエヌ」と読まれる。 | | 化学的特性 | WHITE CRYSTALLINE POWDER | | 使用 | Protecting group for alkenes?
Reactant for:
- Linear SPPS synthesis of ubiquitin derivatives
- Copper-catalyzed cross-coupling reactions of organoboron compounds with primary alkyl halides and pseudohalides
- Intramolecular insertion of alkenes into palladium-nitrogen bonds
- Preparation of (phosphonoacetyl)ornithine to study effect on arginine biosynthetic genes in yeast
- Hetero-Diels-Alder reaction for synthesis of spirocyclic alkaloids
| | 使用 | 9-BBN monomer acts as a selective hydroboration reagent in synthetic organic chemistry. It is employed in Suzuki reactions as well as in the preparation of terminal alcohols by the region selective addition of alkenes followed by oxidative cleavage using hydrogen peroxide. It is also used in copper-catalyzed cross-coupling reactions of organoboron compounds with primary alkyl halides and pseudohalides. It acts as a protecting group for alkenes. Further, it is used as a reactant for Hetero-Diels-Alder reaction for the synthesis of spirocyclic alkaloids. In addition to this, it is used in intramolecular insertion of alkenes into palladium-nitrogen bonds. | | 一般的な説明 | 9-Borabicyclo[3.3.1]nonane is an organic compound, which is generally used as a hydroborating agent. It is thermally stable, less sensitive to oxygen and water when compared to other dialkyl boranes. It is commonly used to prepare aldehydes from alkynes. | | 合成方法 | a) 1,5-シクロオクタジエンにBH3・SMe2を作用さる方法
複製する位置異性体である9-Borabicyclo[2.4.1]nonaneは9-BBNよりも熱力学的に不安定であり、加熱条件下で9-BBNに異性化する。
b)ボラン錯体の代わりにソジウムボロヒドリドとルイス酸を用いる方法
| | 純化方法 | It is available as the solid dimer or in tetrahydrofuran solution. The solid is relatively stable and can be purified by distillation in a vacuum (as dimer) and by recrystallisation from tetrahydrofuran (solubility at room temperature is 9.5%, 0.78M), filter off the solid under N2, wash it with dry pentane and dry it in vacuo at ca 100o. The solid is a dimer (IR 1567cm-1), stable in air (for ca 2 months), and can be heated for 24hours at 200o in an inert atmosphere without loss of hydride activity. It is a dimer in tetrahydrofuran solution also (IR 1567cm-1). It is sensitive to H2O and air (O2) in solution. Its concentration in solution can be determined by reaction with MeOH and measuring the volume of H2 liberated, or it can be oxidised to cis-cyclooctane-1,5-diol (m 73.5-74.5o). [IR: Knights & Brown J Am Chem Soc 90 5280 1968, Brown et al. J Am Chem Soc 96 7765 1974, Brown et al. J Org Chem 41 1778 1976, Brown & Chen J Org Chem 46 3978 1981, Fieser & Fieser Reagents for Org Synth 2 31, 3 24, 10 48, 15 43, 17, 49.] Borane pyridine complex [110 -51 -0] M 92.9, m 8-10o, 10-11o, b 86o/7mm, 100-1 0 1o/12mm, d 4 0.785. Dissolve it in Et2O and wash it with H2O in which it is insoluble. Evaporate the Et2O and distil the residual oil to gives better than 99.8% purity. Its vapour pressure is less than 0.1mm at room temperature. [Taylor et al. J Am Chem Soc 77 1506 1955, Beilstein 20 IV 2235.] |
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