R 3 B NaOH, 25 oC 3 R + Na 3 BO 3
oxidation
OH
H 2 O 2
- The alkyl migration takes place with retention of configuration of the alkyl
group which leads to the formation of a trialkyl borate, an ester, B(OR) 3.
- The ester then undergoes basic hydrolysis to produce three molecules of alcohol
and a borate ion.
B(OR) 3 + 3 OH– H^2 O 3 R–OH + BO 3 3–
- The net result of hydroboration-oxidation is an anti-Markovnikov addition of
water to a double bond.
- Two complementary orientations for the addition of water to a double bond:
- Acid-catalyzed hydration (or oxymercuration-demercuration) of 1-hexene:
CH 3 CH 2 CH 2 CH 2 CH CH 2
H 3 O+, H 2 O
OH
CH 3 CH 2 CH 2 CH 2 CHCH 3
1-Hexene 2-Hexanol
2) Hydroboration-oxidation of 1-hexene:
CH 3 CH 2 CH 2 CH 2 CH CH 2 1.THF:BH^3
1-Hexene 1-Hexanol (90%)
- H 2 O 2 , OH− CH^3 CH^2 CH^2 CH^2 CH^2 CH^2 OH
3) Other examples of hydroboration-oxidation of alkenes:
C CHCH 3
CH 3
H 3 C H 3 C CCHCH 3
H
CH 3
OH
H 2 O 2 , OH−
2-Methyl-2-butene 3-Methyl-2-butanol (59%)
- THF: H 3
B