Hydroboration–oxidation reaction
In organic chemistry, the hydroboration–oxidation reaction is a two-step organic reaction that converts an alkene into a neutral alcohol by the net addition of water across the double bond.[1] The hydrogen and hydroxyl group are added in a syn addition leading to cis stereochemistry. Hydroboration–oxidation is an anti-Markovnikov reaction, with the hydroxyl group attaching to the less-substituted carbon. The reaction was first reported by Herbert C. Brown in the late 1950s[2] and it was recognized in his receiving the Nobel Prize in Chemistry in 1979.
The general form of the reaction is as follows:
Tetrahydrofuran (THF) is the archetypal solvent used for hydroborations.
Contents
1 Mechanism and scope
1.1 Hydroboration step
1.2 Oxidation step
2 Alkyne hydroboration
3 Related reactions
3.1 Oxymercuration
3.2 Other boron-mediated C-X bond forming reactions
4 References
5 External links
Mechanism and scope
Hydroboration step
In the first step, borane (BH3) adds to the double bond, transferring one of the hydrogen atoms to the carbon adjacent to the one that becomes bonded to the boron. This hydroboration is repeated two additional times, successively reacting each B–H bond so that three alkenes add to each BH3. The resulting trialkylborane is treated with hydrogen peroxide in the second step. This process replaces the B-C bonds with HO-C bonds. The boron reagent is converted to boric acid. The reaction was originally described by H.C. Brown in 1957 for the conversion of 1-hexene into 1-hexanol.[3]
Hexanol synthesis
Knowing that the group containing the boron will be replaced by a hydroxyl group, it can be seen that the initial hydroboration step determines the regioselectivity. Hydroboration proceeds in an antimarkovnikov manner. The reaction sequence is also stereospecific, giving syn addition (on the same face of the alkene): the hydroboration is syn-selective and the oxidation replaces the boron with hydroxyl having the same geometric position. Thus 1-methylcyclopentene reacts with diborane predominantly to give trans-1-hydroxy-2-methylcyclpentane[4]—the newly added H and OH are cis to each other.
Until all hydrogens attached to boron have been transferred away, the boron group BH2 will continue adding to more alkenes. This means that one mole of hydroborane will undergo the reaction with three moles of alkene. Furthermore, it is not necessary for the hydroborane to have more than one hydrogen. For example, reagents of the type R2BH are commonly used, where R can represents the remainder of the molecule. Such modified hydroboration reagents include 9-BBN, catecholborane, and disiamylborane.
Oxidation step
In the second step of the reaction sequence, the nucleophilic hydroperoxide anion attacks the boron atom. Alkyl migration to oxygen gives the alkyl borane with retention of stereochemistry (in reality, the reaction occurs via the trialkyl borate B(OR)3, rather than the monoalkyl borinic ester BH2OR).
Hydroboration–oxidation mechanism
The 'H' atom in the reaction comes from B2H6, the 'O' atom comes from hydrogen peroxide (H2O2) whereas the O attached 'H'atom comes from the solvent (refer mechanism).
Alkyne hydroboration
A hydroboration reaction also takes place on alkynes. Again the mode of action is syn and secondary reaction products are aldehydes from terminal alkynes and ketones from internal alkynes. In order to prevent hydroboration across both the pi-bonds, a bulky borane like disiamyl (di-sec-iso-amyl) borane is used.[5]
Hydroboration–oxidation of terminal alkyne
Related reactions
Oxymercuration
Oxymercuration–reduction is another reaction that converts an alkene into an alcohol. Unlike hydroboration–oxidation, oxymercuration-reduction is not stereospecific. Further, oxymercuration–reduction is a Markovnikov reaction. Therefore, oxymercuration–reduction and hydroboration–oxidation are complementary because they add with opposite regiochemistry.
Other boron-mediated C-X bond forming reactions
Amines can be obtained from the intermediate organoborane by action of chloramine.[6] Reaction with iodine or bromine afford the corresponding alkyl halides.[7][8] Reaction with a carboxylic acid converts organoboranes to simple alkyl groups by replacement of the boron atom with a hydrogen.
References
^ Loudon, Marc G. (2002). "Addition Reactions of Alkenes.". Organic Chemistry (Fourth ed.). New York: Oxford University Press. pp. 168–172. ISBN 0-19-511999-1..mw-parser-output cite.citationfont-style:inherit.mw-parser-output qquotes:"""""""'""'".mw-parser-output code.cs1-codecolor:inherit;background:inherit;border:inherit;padding:inherit.mw-parser-output .cs1-lock-free abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-lock-limited a,.mw-parser-output .cs1-lock-registration abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-lock-subscription abackground:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registrationcolor:#555.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration spanborder-bottom:1px dotted;cursor:help.mw-parser-output .cs1-hidden-errordisplay:none;font-size:100%.mw-parser-output .cs1-visible-errorfont-size:100%.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-formatfont-size:95%.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-leftpadding-left:0.2em.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-rightpadding-right:0.2em
^ Brown, H. C.; Zweifel, G. (1959). "A STEREOSPECIFIC CIS HYDRATION OF THE DOUBLE BOND IN CYCLIC DERIVATIVES". Journal of the American Chemical Society. 81: 247. doi:10.1021/ja01510a059.
^ Brown, H.; Rao, B. C. (1957). "Communications – Selective Conversion of Olefins into Organoboranes Through Competitive Hydroboration, Isomerization and Displacement Reactions". Journal of Organic Chemistry. 22 (9): 1137. doi:10.1021/jo01360a626.
^ Hawthorne, M. F. (1961). "Amine Boranes. VIII. The Hydroboration of Terminal Olefins, Dienes and Terminal Acetylenes with Trimethylamine t-Butylborane". Journal of the American Chemical Society. 83 (11): 2541–2544. doi:10.1021/ja01472a027.
^ Brown, H. C.; Gupta, S. K. (1972). "Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration". Journal of the American Chemical Society. 94 (12): 4370. doi:10.1021/ja00767a072.
^ Brown, H. C.; Heydkamp, W. R.; Breuer, E.; Murphy, W. S. (1964). "The Reaction of Organoboranes with Chloramine and with Hydroxylamine-O-sulfonic Acid. A Convenient Synthesis of Amines from Olefins via Hydroboration". Journal of the American Chemical Society. 86 (17): 3565. doi:10.1021/ja01071a036.
^ Brown, H. C.; Rathke, M. W.; Rogic, M. M. (1968). "A fast reaction of organoboranes with iodine under the influence of base. A convenient procedure for the conversion of terminal olefins into primary iodides via hydroboration-iodination". Journal of the American Chemical Society. 90 (18): 5038. doi:10.1021/ja01020a056.
^ Brown, H. C.; Lane, C. F. (1970). "Base-induced reaction of organoboranes with bromine. Convenient procedure for the anti-Markovnikov hydrobromination of terminal olefins via hydroboration-bromination". Journal of the American Chemical Society. 92 (22): 6660. doi:10.1021/ja00725a057.
External links
- Organic Chemistry Portal. Hydroboration (including recent literature). https://www.organic-chemistry.org/namedreactions/brown-hydroboration.shtm
