Borane dimethylsulfide (BMS) is a chemical compound with the chemical formula BH3·S(CH3)2. It is an adduct between borane molecule (BH3) and dimethyl sulfide molecule (S(CH3)2). It is a complexed borane reagent that is used for hydroborations and reductions. The advantages of BMS over other borane reagents, such as borane-tetrahydrofuran, are its increased stability and higher solubility.[1] BMS is commercially available at much higher concentrations than its tetrahydrofuran counterpart (10 M) and does not require sodium borohydride as a stabilizer, which could result in undesired side reactions.[2] In contrast, BH3·THF requires sodium borohydride to inhibit reduction of THF to tributyl borate (B(OCH2CH2CH2CH3)3).[2] BMS is soluble in most aprotic solvents.
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| Other names
BMS, Borane-dimethyl sulfide
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| Identifiers | |
3D model (JSmol)
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| ECHA InfoCard | 100.032.998 |
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CompTox Dashboard (EPA)
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| Properties | |
| BH3·S(CH3)2 | |
| Molar mass | 75.96 g/mol |
| Appearance | colorless liquid |
| Density | 0.801 g/mL |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Preparation and structure
editAlthough usually purchased, BMS can be prepared by absorbing diborane into dimethyl sulfide:[3]
- B2H6 + 2 S(CH3)2 → 2 BH3·S(CH3)2
It can be purified by bulb to bulb vacuum transfer. Although a structure of BMS has not been determined crystallographically, (pentafluorophenyl)-borane dimethylsulfide (C6F5BH2·S(CH3)2), has been examined by X-ray crystallography.[4] The boron atom adopts a tetrahedral molecular geometry.
Reactions
editHydroborations
editDue to the experimental ease of its use, BMS has become common in hydroboration reactions.[5] In hydroborations with BMS, the dimethylsulfide dissociates in situ, liberating diborane, which rapidly adds to the unsaturated bonds. The resulting organoborane compounds are useful intermediates in organic synthesis. Boranes add to alkenes in an anti-Markovnikov fashion and allow conversion of alkynes to the corresponding cis-alkenes.
Reductions
editBMS has been employed for the reduction of many functional groups. Reductions of aldehydes, ketones, epoxides, esters, and carboxylic acids give the corresponding alcohols. Lactones are reduced to diols, and nitriles are reduced to amines. Acid chlorides are not reduced by BMS.
Borane dimethylsulfide is one of the most common bulk reducing agents used in the Corey–Itsuno reduction. The dimethylsulfide ligand attenuates the reactivity of the borane. Activation by the nitrogen of the chiral oxazaborolidine[clarification needed] catalyst of the stoichiometric reducing agent allows for asymmetric control of the reagent.[clarification needed] In general BMS does not lead to significantly greater enantiomeric selectivities than borane-THF, however its increased stability in the presence of moisture and oxygen makes it the reagent of choice for the reduction.[6]
Safety
editBorane dimethylsulfide is flammable and reacts readily with water to produce a flammable gas. It also has an unpleasant smell.[7]
References
edit- ^ Hutchins, Robert O.; Cistone, Frank (1981). "Utility and Applications of Borane Dimethylsulfide in Organic Synthesis. A Review". Organic Preparations and Procedures International. 13 (3–4): 225. doi:10.1080/00304948109356130.
- ^ a b Kollonitisch, J. (1961). "Reductive Ring Cleavage of Tetrahydrofurans by Diborane". J. Am. Chem. Soc. 83 (6): 1515. doi:10.1021/ja01467a056.
- ^ Braun, L. M.; Braun, R. A.; Crissman, R.; Opperman, M.; Adams, R. M. (1971). "Dimethyl Sulfide-Borane. A Convenient Hydroborating Reagent". J. Org. Chem. 36 (16): 2388–2389. doi:10.1021/jo00815a047.
- ^ Fuller, Anna-Marie; Hughes, David L.; Lancaster, Simon J.; White, Callum M. (2010). "Synthesis and Structure of the Dimethyl Sulfide Adducts of Mono- and Bis(pentafluorophenyl)borane". Organometallics. 29 (9): 2194. doi:10.1021/om100152v.
- ^ Atsushi Abiko (1925). "Dicyclohexylboron Trifluoromethylsulfonate". Organic Syntheses. 79: 103; Collected Volumes, vol. 10, p. 273.
- ^ Corey, E.J.; Helal, C. J. (1998). "Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method". Angew. Chem. Int. Ed. 37 (15): 1986–2012. doi:10.1002/(SICI)1521-3773(19980817)37:15<1986::AID-ANIE1986>3.0.CO;2-Z. PMID 29711061.
- ^ "Sigma-Aldrich Material Safety Data Sheet". www.sigmaaldrich.com/. Retrieved 29 November 2014.