Hydrogen Peroxide → 4,4-Dimethyl-5-methoxypentan-1-ol

HRID 1441047Notes

Reaction equation

HRID 1441047 reaction equation
B.CSC.[CH3:5][C:6]([CH3:13])([CH2:10][O:11][CH3:12])[CH2:7][CH:8]=[CH2:9].[OH-:14].[Na+].OO>CCCCCC.O.C(O)C>[CH3:5][C:6]([CH3:13])([CH2:10][O:11][CH3:12])[CH2:7][CH2:8][CH2:9][OH:14]

Participants

8

Procedure

Borane-methyl sulphide complex (2.76 ml., 2M solution in tetrahydrofuran, Aldrich) was added to 4,4-dimethyl-5-methoxypent-1-ene (1.9 g.) in dry hexane (50 ml.) under nitrogen at 0°. The mixture was stirred at 20° for 2 hours and ethanol (15 ml.) was added. 2N Aqueous sodium hydroxide solution (6.0 ml.) was then added. The mixture was cooled to 0° and hydrogen peroxide (5.3 ml., 30% aqueous solution) was added dropwise. The mixture was refluxed for 1 hour, cooled and poured into iced water (100 ml.). The aqueous mixture was extracted with diethyl ether. The ethereal extracts were washed with water and dried over anhydrous magnesium sulphate. The solvent was removed in vacuo and 4,4-dimethyl-5-methoxypentan-1-ol was obtained as a colourless oil (1.12 g).

Workup

  1. temperatureThe mixture was cooled to 0°
  2. temperatureThe mixture was refluxed for 1 hour
  3. temperaturecooled
  4. extractionThe aqueous mixture was extracted with diethyl ether
  5. washThe ethereal extracts were washed with water
  6. dry with materialdried over anhydrous magnesium sulphate
  7. customThe solvent was removed in vacuo

Sources & evidence

ORD record
ord-3b55145f72b0482181661c49c40077c0
Source dataset
uspto-grants-1996_03
Patent number
US05502073

Reaction notes

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