Diisopinocampheylborane

Diisopinocampheylborane
Names
IUPAC name
Bis{(1S,2S,3S,5R)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-yl} borane
Other names
(+)-Di-3-pinanylborane; Diisopinocampheylborane; Ipc2BH
Identifiers
3D model (JSmol)
Abbreviations Ipc2BH
ChemSpider
Properties
C20H35B
Molar mass 286.31 g·mol−1
Appearance Colorless solid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Diisopinocampheylborane is an organoborane that is useful for asymmetric synthesis. This colourless solid is the precursor to a range of related reagents. The compound was reported in 1961 by Zweifel and Brown in a pioneering demonstration of asymmetric synthesis using boranes. The reagent is mainly used for the synthesis of chiral secondary alcohols.

Preparation

Diisopinocampheylborane was originally prepared by hydroboration of excess α-pinene with borane,[1] but it is now more commonly generated from borane-methyl sulfide (BMS).[2]

The compound can be isolated as a solid. Because it is quite air sensitive to water and air, this reagent is thus often generated in situ and used as a solution.

Diisopinocampheylborane is monomeric, in contrast to diborane and many of its less bulky analogues.

Reactions

Oxidation of diisopinocampheylborane with basic hydrogen peroxide gives isopincampheol. Methanolysis gives methoxydiisopinocampheylborane

Hydroboration

Because of the large size of the α-pinenyl substituents, diisopinocampheylborane only hydroborates unhindered alkenes. These reactions proceed with high enantioselectivity. 2-Butene, 2-pentene, 3-hexene are converted to the respective chiral alcohols in high ee's.[3][3] Norbornene under the same conditions gave an 83% ee. Hetrocycles (dihydrofuran, dihydrothiophene, dihydropyrrole, tetrahydropyran) give the alcohols in ≥99% ee; the high ee's reflect their constrained conformations.[4]

It adds to alkynes to form the corresponding vinyldiisopinocampheylboranes

In a highly stereoselective reaction, allyldiisopinocampheylboranes converts aldehydes to the homologated alcohols, rapidly even at -100 °C.[5] The alkyldiisopinocampheylboranes, which result from the addition to alkenes, usefully react with a range of different reagents. Hydroxylamine-O-sulfonic acid provides 3-pinanamine.[6]

Also useful is the reaction of diisopinocampheylborane with an aldehyde (RCHO) to give the chiral boronic ester, (isopinocampheyl)2BOCH2(R), which can be further used is a number of reactions e.g. Suzuki reaction.[3]

Diisopinocampheylchloroborane
Alpine borane

Treatment of diisopinocampheylborane with TMEDA give the crystalline adduct of monoisopinocampheylborane. This adduct reacts with boron trifluoride to liberate the monoisopinocampheylborane (IpcBH2) in 100% ee.[7] Monoisopinocampheylborane reacts with a variety of alkenes.[3] Two other reagents have been developed for the hydroboration of ketones:

In the above mechanism where G=O and R is Ipc and Cl or 9-Borabicyclononane. Diisopinocampheylchloroborane (Ipc2BCl) is produced by treating diisopinocampheylborane with hydrogen chloride. The chloride is reported to be more stable that the trialkyl boranes,[3] it works well with aryl alkyl ketones and tert-butyl aklyl ketones. Diisopinocampheylchloroborane is often complementary with diisopinocampheylborane, where one provides the R enantiomer and the other the S, the enantioselectivity is typically very high.[8][9]

Alpine-borane is produced by hydroborating α-pinene with 9-borabicyclononane.[3] Both of these reagents can be improved upon by using 2-ethylapopinene in place of α-pinene, 2-ethylapopinene has an ethyl group in place of the methyl in α-pinene. The additional steric bulk improves the stereoselectivity of the reduction.

Diisopinocampheylborane reacts with methanol to give diisopinocampheylmethoxyborane, which in turn reacts with an allyl or crotyl Grignard reagent to give B-allyldiisopinocampheylborane. This can then undergo an asymmertric allylboration to give a chiral homologated alcohol, which is a useful building block in a chiral synthesis.

References

  1. ↑ Brown, Herbert C.; Yoon, Nung Min (1976). "Hydroboration. 44. Diisopinocampheylborane of High Optical Purity. Asymmetric Synthesis via Hydroboration with Essentially Complete Asymmetric Induction". Israel Journal of Chemistry. 15 (1-2): 12–16. ISSN 0021-2148. doi:10.1002/ijch.197600004.
  2. ↑ C. F. Lane, J. J. Daniels (1972). "(−)-Isopincampheol". Org. Synth. 52: 59.; Coll. Vol., 6, p. 719
  3. 1 2 3 4 5 6 Brown, Herbert C.; George Zweifel (1961). "Hydroboration as a convenient procedure for the asymmetric synthesis of alcohols of high optical purity". J. Am. Chem. Soc. 83 (2): 486–487. doi:10.1021/ja01463a055.
  4. ↑ Brown, Herbert C.; Veeraraghavan Ramachandran (1991). "The boron approach to asymmertric synthesis". Pure & Appl. Chem. 63 (3): 307–316. doi:10.1351/pac199163030307.
  5. ↑ Raj K. Dhar, Kanth V. B. Josyula, Robert Todd “Diisopinocampheylborane” in Encyclopedia of Reagents for Organic Synthesis, 2006, John Wiley & Sons, New York. doi:10.1002/047084289X.rd248.pub2. Article Online Posting Date: September 15, 2006
  6. ↑ Michael W. Rathke, Alan A. Millard. (1978). "Boranes in functionalization of olefins to amines: 3-Pinanamine". Org. Synth. 58: 32.; Coll. Vol., 6, p. 943
  7. ↑ Brown, Herbert C.; John R. Schwier; Bakthan Singaram (1978). "Simple synthesis of monoisopinocampheylborane of high optical purity". J. Org. Chem. 43 (32): 4395–4397. doi:10.1021/jo00416a042.
  8. ↑ Ramachandran, P.Veeraraghavan; Chen, Guang-Ming; Brown, Herbert C. (1996). "Efficient general asymmetric syntheses of 3-substituted 1(3H)-isobenzofuranones in very high enantiomeric excess". Tetrahedron Letters. 37 (13): 2205–2208. ISSN 0040-4039. doi:10.1016/0040-4039(96)00260-2.
  9. ↑ Ramachandran, V. P.; S. Pitre; Herbert C. Brown (2002). "Selective Reductions. 59. Effective Intramolecular Asymmetric Reductions of α-,β and γ-Keto Acids with Diisopinocampheylborane and Intermolecular Asymmetric Reductions of the Corresponding Esters with B-Chlorodiisopinocampheylborane". J. Org. Chem. 67 (15): 5315–5319. doi:10.1021/jo025594y.
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